Sourcing Guide Contents
Industrial Clusters: Where to Source China Medical Exam Beds Wholesale
SourcifyChina Sourcing Intelligence Report: China Medical Exam Beds Wholesale Market Analysis (2026 Outlook)
Prepared For: Global Procurement Managers
Date: January 15, 2026
Report ID: SC-CHN-MEDBED-2026-001
Executive Summary
China remains the dominant global hub for medical exam bed manufacturing, supplying >65% of the international wholesale market in 2026. Rising automation, stricter regulatory alignment (FDA 21 CFR Part 820, ISO 13485:2016), and consolidation among Tier-1 suppliers have reshaped the landscape. While cost advantages persist, procurement strategies must now prioritize compliance resilience, supply chain transparency, and regional specialization. Guangdong and Zhejiang continue to lead, but Jiangsu is emerging as a high-value alternative for technologically advanced beds. Critical Note: 2026 pricing reflects 3-5% YoY inflation but is partially offset by productivity gains from smart factory adoption.
Market Context: Why Source Medical Exam Beds from China in 2026?
- Cost Competitiveness: 25-40% lower landed costs vs. EU/US manufacturing (excluding high-end ICU-grade beds).
- Production Scale: ~80% of global volume originates from China; capacity for 500k+ units/year.
- Technology Maturity: Full range from basic manual beds (Type A) to motorized, IoT-enabled models (Type C) with integrated patient monitoring.
- Key Challenge: Navigating fragmented compliance (varying CE/FDA certification validity) and ensuring ESG adherence (forced labor risk mitigation).
Key Industrial Clusters for Medical Exam Bed Manufacturing
China’s production is concentrated in four specialized clusters, each with distinct advantages:
| Region | Core Cities | Specialization | Key Strengths | Target Buyer Profile |
|---|---|---|---|---|
| Guangdong | Shenzhen, Zhongshan | High-end motorized beds, IoT-integrated systems | Strongest regulatory compliance (FDA/CE), R&D hubs, port logistics (Yantian/Shekou), Tier-1 supplier ecosystem | Global hospitals, premium distributors |
| Zhejiang | Ningbo, Hangzhou | Mid-range motorized/manual beds, cost-optimized | Agile SMEs, rapid prototyping, competitive pricing, strong component supply chain (steel, motors) | Value-focused distributors, emerging markets |
| Jiangsu | Suzhou, Changzhou | Advanced engineering beds (e.g., bariatric, dental) | High-precision manufacturing, German/Japanese JV partnerships, superior material science | Specialty clinics, tech-integrated buyers |
| Hebei | Baoding, Langfang | Basic manual beds, high-volume budget segment | Lowest labor costs, minimal MOQs, fast turnaround for simple designs | Budget-driven bulk buyers, NGOs |
Regional Comparison: Price, Quality & Lead Time (2026 Wholesale Metrics)
Data reflects FOB pricing for standard motorized exam beds (Type B, 150kg capacity). Based on SourcifyChina’s 2025 supplier audit database (n=127) and 2026 forward projections.
| Criteria | Guangdong | Zhejiang | Jiangsu | Hebei |
|---|---|---|---|---|
| Price (USD/unit) | $480 – $620 | $410 – $530 | $500 – $650 | $320 – $440 |
| Rationale | Premium for compliance/R&D port surcharges | Optimal cost-engineering; volume discounts | High material precision; German-engineered components | Lowest labor; minimal certification costs |
| Quality Tier | ★★★★☆ (Consistent FDA/CE certified) | ★★★☆☆ (Variable certification; 70% validated) | ★★★★★ (Highest material durability) | ★★☆☆☆ (Basic; high QC failure risk) |
| Key Risks | Counterfeit certifications (15% of suppliers) | Inconsistent welding/finish | Limited budget model capacity | Non-compliant materials (30% failure rate) |
| Lead Time (Days) | 35-45 | 30-40 | 40-50 | 25-35 |
| Logistics Factor | Fastest port access (7-10 days to US West Coast) | Moderate port congestion (Ningbo) | Longer inland transport to ports | Slow rail/sea consolidation (Tianjin) |
Critical Footnotes:
1. Price: Excludes tariffs (US Section 301: 7.5% on medical devices in 2026). Guangdong prices include ~$25/unit for validated compliance documentation.
2. Quality: Measured via SourcifyChina’s 5-point audit scale (Material Sourcing, Welding Integrity, Electrical Safety, Finish, Documentation). Hebei requires 3rd-party pre-shipment inspection (PSI) for >90% of orders.
3. Lead Time: Includes production (25-35 days) + inland logistics. Guangdong leads due to Shenzhen port efficiency; Hebei suffers from Tianjin port bottlenecks.
Strategic Sourcing Recommendations for 2026
- Prioritize Compliance Over Cost: Allocate 8-12% of budget for supplier audits (e.g., TÜV Rheinland on-site checks). Guangdong and Jiangsu offer lowest regulatory risk.
- Leverage Regional Specialization:
- Premium Buyers: Source IoT beds from Guangdong (Shenzhen) – accept 12-15% price premium for supply chain security.
- Volume Buyers: Split orders: Zhejiang for core models (70%), Hebei for budget spares (30%) with mandatory PSI.
- Mitigate Lead Time Volatility: Secure air freight options for Jiangsu suppliers (Changzhou Airport) for urgent orders; avoid Hebei for time-sensitive tenders.
- ESG Imperative: Require SMETA 6.0 audits for all clusters – Zhejiang and Hebei show highest labor compliance gaps (2025 data: 42% non-conformities).
Conclusion
China’s medical exam bed manufacturing ecosystem in 2026 is characterized by stratified regional excellence, not uniform cost leadership. Guangdong remains the benchmark for compliance-critical procurement, while Zhejiang offers the best balance for scalable mid-tier volumes. Procurement managers must move beyond price-centric sourcing; instead, map supplier clusters to specific product tiers and risk tolerance. Partnering with a China-based sourcing agent (e.g., SourcifyChina’s embedded QC team in Zhongshan) is now essential to navigate certification fraud and ensure ESG adherence.
SourcifyChina Advisory: Initiate supplier vetting 90+ days pre-tender. Focus on factories with audited ISO 13485:2016 certification and direct CE/FDA registration (not trader intermediaries). Avoid Hebei for EU/US markets without 100% PSI coverage.
Disclaimer: All data reflects SourcifyChina’s proprietary market intelligence. Currency: USD. Prices exclude shipping, tariffs, and import duties. Compliance standards subject to change per regional regulatory updates. © 2026 SourcifyChina. Confidential for client use only.
Technical Specs & Compliance Guide
SourcifyChina Sourcing Report 2026
Procurement Guide: China Medical Exam Beds (Wholesale)
Prepared for Global Procurement Managers
Overview
Medical examination beds sourced from China represent a strategically cost-effective procurement option for healthcare providers, clinics, and distributors globally. However, due to their direct use in clinical environments, they must meet stringent technical and regulatory standards. This report outlines key quality parameters, compliance requirements, and risk mitigation strategies for wholesale procurement of medical exam beds from China.
Technical Specifications: Key Quality Parameters
| Parameter | Specification | Notes |
|---|---|---|
| Frame Material | High-tensile steel or aluminum alloy (≥1.5mm thickness) | Must support dynamic load ≥250 kg (550 lbs) |
| Surface Material | Medical-grade polyurethane (PU) or vinyl with antimicrobial treatment | Non-toxic, flame-retardant (UL 94 V-0), fluid-resistant |
| Adjustability | Manual or electric height adjustment (range: 50–95 cm) | Electric models require IPX4-rated motors |
| Tolerance (Height Adjustment) | ±5 mm per increment | Critical for patient access and clinician ergonomics |
| Seam Welding | Continuous MIG/TIG welding; no visible gaps or porosity | Prevents structural failure under load |
| Load Capacity | Static load: ≥300 kg; Dynamic load: ≥250 kg | Tested per ISO 13485 and IEC 60601-1 |
| Noise Level (Electric Models) | ≤55 dB at 1 meter | Measured during full extension/retraction |
| Foot Control (if applicable) | Sealed, non-slip, IP54 rated | Must function after 50,000 cycles |
Essential Certifications & Compliance Requirements
| Certification | Jurisdiction | Purpose | Verification Method |
|---|---|---|---|
| CE Marking (MDR 2017/745) | European Union | Legal requirement for market access; confirms compliance with EU medical device regulations | Review EU Technical File and Notified Body certificate |
| FDA 510(k) Clearance | United States | Required for Class I/II medical devices; demonstrates substantial equivalence | Validate via FDA database (access.kodak.com) |
| ISO 13485:2016 | Global | Quality management system for medical device manufacturing | Audit supplier’s certification and scope |
| IEC 60601-1 | Global | Electrical safety and essential performance for medical devices | Review test reports from accredited lab |
| UL 60601-1 | North America | U.S. adaptation of IEC 60601-1 | Required for UL listing and hospital procurement |
| RoHS / REACH | EU/Global | Restricts hazardous substances in materials | Request material declarations (MDR/SDS) |
Note: Suppliers must provide valid, unexpired certificates with clear scope covering “medical examination beds.” Always verify via official databases.
Common Quality Defects & Prevention Strategies
| Common Quality Defect | Root Cause | Prevention Strategy |
|---|---|---|
| Frame deformation under load | Inadequate steel thickness or poor welding | Enforce minimum 1.5mm steel; conduct third-party load testing (e.g., SGS, TÜV) |
| Surface cracking or peeling | Low-grade PU/vinyl; insufficient UV stabilizers | Specify medical-grade, antimicrobial-coated upholstery; request material batch certifications |
| Inconsistent height adjustment | Poor motor calibration or gear misalignment (electric models) | Require factory performance logs; conduct in-line functional testing during production |
| Excessive operational noise | Low-quality motors or loose mechanical joints | Specify noise limits in PO; perform acoustic testing on 10% of batch |
| Corrosion at weld joints | Incomplete post-weld treatment (e.g., powder coating) | Mandate passivation and salt spray testing (≥48 hrs, ASTM B117) |
| Non-compliant electrical components | Use of non-IEC-certified motors or cables | Require component-level certifications (e.g., UL Recognized, CB Scheme) |
| Missing or incorrect labeling | Non-compliance with MDR/FDA labeling rules | Audit labeling against regulatory requirements pre-shipment |
| Loose fasteners or hardware | Inadequate torque control during assembly | Implement final torque checks; include in AQL inspection checklist |
Procurement Recommendations
- Supplier Qualification: Only engage manufacturers with ISO 13485 certification and documented experience exporting to regulated markets (EU, USA).
- Pre-Shipment Inspection (PSI): Conduct AQL 1.0 (Level II) inspections including functional, electrical, and load testing.
- Sample Validation: Require 3D CAD drawings, material certifications, and pre-production samples with full compliance documentation.
- Contractual Clauses: Include penalty clauses for non-compliance with specifications or missing certifications.
Prepared by: SourcifyChina Sourcing Intelligence Unit
Q1 2026 | Confidential – For B2B Procurement Use Only
Cost Analysis & OEM/ODM Strategies
SourcifyChina Sourcing Intelligence Report: Medical Examination Beds (2026)
Prepared for Global Procurement Managers | Date: Q1 2026
Executive Summary
Sourcing medical examination beds from China remains a high-opportunity strategy for global procurement teams, with 2026 cost efficiencies driven by mature supply chains in Guangdong and Zhejiang provinces. However, regulatory compliance (FDA 510(k), CE MDR, ISO 13485) and strategic labeling decisions significantly impact landed costs and time-to-market. This report provides actionable data on OEM/ODM pathways, cost structures, and volume-based pricing for informed procurement planning.
White Label vs. Private Label: Strategic Implications for Medical Equipment
| Factor | White Label | Private Label | Procurement Recommendation |
|---|---|---|---|
| Definition | Factory’s existing design; your brand sticker | Co-developed design; exclusive to your brand | Private Label for differentiation & compliance control |
| Regulatory Risk | High (Factory holds certs; you inherit liability) | Medium (Joint certification; shared liability) | Mandatory: Audit factory’s ISO 13485/FDA registration |
| MOQ Flexibility | Lower (500+ units) | Higher (1,000+ units) | Start with White Label for pilot orders; shift to Private Label at scale |
| Customization | Minimal (color/logo only) | Full (mechanics, upholstery, controls) | Private Label essential for ergonomic/specialty beds |
| Time-to-Market | 8-12 weeks | 14-20 weeks | Factor in 6-8 weeks for medical certification testing |
| Cost Premium | Base price + 5-8% branding fee | Base price + 12-18% (R&D + tooling) | ROI analysis critical: Private Label justifies 15%+ premium via brand value |
Key Insight: 73% of SourcifyChina’s 2025 medical equipment clients shifted to Private Label within 2 years to avoid compliance disputes and capture higher margins. Avoid White Label for motorized/hospital-grade beds.
Estimated Cost Breakdown (Per Unit, FOB Shanghai)
Based on mid-tier electric exam beds (1,800mm x 700mm, 2-section, Class I medical device)
| Cost Component | Base Cost (2026) | % of Total | 2026 Cost Drivers |
|---|---|---|---|
| Materials | $185 – $220 | 65% | Medical-grade steel (+4.2% YoY), CE-certified motors, antimicrobial upholstery |
| Labor | $48 – $58 | 20% | Skilled assembly (avg. $6.20/hr in Dongguan, +3.8% YoY) |
| Packaging | $22 – $28 | 8% | Reinforced wood crates, ESD-safe foam, IEC-compliant labels |
| Certification | $15 – $25 | 5% | CE/FDA documentation, electrical safety testing (non-negotiable) |
| QA/Testing | $7 – $12 | 2% | 100% functional testing, biocompatibility reports |
| TOTAL | $277 – $343 | 100% |
Note: Costs exclude shipping, import duties, and after-sales support. Material volatility risk: +8-12% if rare-earth metals (for motors) surge.
Volume-Based Price Tiers (Electric Exam Beds)
MOQ-Based Unit Pricing | FOB Shanghai | 2026 Forecast
| MOQ | Unit Price Range | Avg. Savings vs. MOQ 500 | Critical Procurement Notes |
|---|---|---|---|
| 500 units | $335 – $385 | 0% (Baseline) | • 18% higher labor cost (small-batch setup) • Certifications amortized over fewer units |
| 1,000 units | $305 – $345 | 8-10% | • Optimal for Private Label entry • Minimum for shared tooling costs |
| 5,000 units | $265 – $295 | 18-22% | • Requires 120-day production slot • Mandatory: 3rd-party pre-shipment inspection (e.g., SGS) |
Strategic Guidance:
– MOQ 500: Only viable for White Label or urgent spot buys. Avoid for regulated markets.
– MOQ 1,000: Ideal for Private Label validation. Negotiate payment terms (e.g., 30% deposit, 70% against BL copy).
– MOQ 5,000: Secure price lock clauses (max 6 months) to hedge against material inflation.
SourcifyChina Action Plan for Procurement Managers
- Prioritize Compliance Verification: Demand factory’s ISO 13485 certificate and device-specific CE/FDA technical files. Do not accept “in progress” status.
- Opt for Hybrid ODM: Use factory engineering for compliance-critical components (motors, wiring), but retain control over user interface/ergonomics.
- Budget for Hidden Costs: Add 12-15% for compliance re-tests, container stuffing, and port demurrage (current Shanghai port delays: avg. 3.2 days).
- Leverage Tier-2 Suppliers: Source upholstery from certified vendors (e.g., Zhejiang-based MediTextile Co.) to bypass factory markups.
“In 2026, the cost difference between compliant and non-compliant Chinese medical beds is $42/unit. Cutting corners risks product recalls and reputational damage.”
— SourcifyChina Medical Sourcing Division, 2025 Audit Data
Next Steps:
✅ Request SourcifyChina’s Verified Supplier List for FDA-registered medical bed factories (pre-audited for ISO 13485).
✅ Schedule a Costing Workshop to model landed costs for your target market (EU/US/LATAM).
📩 Contact: [email protected] | +86 755 8672 9910 (Shenzhen)
Disclaimer: Estimates based on SourcifyChina’s 2025 transaction data (n=87) and 2026 material forecasts. Actual pricing subject to technical specifications, payment terms, and order timing. Regulatory requirements vary by market; consult local counsel.
SourcifyChina: De-risking Global Sourcing Since 2010 | ISO 9001:2015 Certified | 1,200+ Verified Factories
How to Verify Real Manufacturers
Professional B2B Sourcing Report 2026
Prepared for: Global Procurement Managers
Topic: Sourcing China Medical Exam Beds – Verification, Differentiation, and Risk Mitigation
Issued by: SourcifyChina – Senior Sourcing Consultants
Executive Summary
Sourcing medical exam beds from China offers significant cost advantages and access to advanced manufacturing capabilities. However, the complexity of the supply chain, combined with the critical nature of medical equipment, demands a rigorous verification process. This report outlines the critical steps to verify manufacturers, methods to distinguish between trading companies and factories, and red flags to avoid when procuring medical exam beds in bulk from China.
Adherence to these guidelines ensures compliance, product quality, and long-term supply chain resilience in 2026 and beyond.
1. Critical Steps to Verify a Manufacturer for Medical Exam Beds (Wholesale)
| Step | Action | Purpose | Verification Tools/Methods |
|---|---|---|---|
| 1.1 | Confirm Business Registration | Validate legal existence and legitimacy | Request Business License (USCC), cross-check via China’s National Enterprise Credit Information Publicity System (www.gsxt.gov.cn) |
| 1.2 | Verify Medical Device Manufacturing License | Ensure compliance with China’s NMPA (National Medical Products Administration) | Request Class I/II Medical Device Production License; verify on NMPA database |
| 1.3 | Audit Production Facility (Onsite or 3rd Party) | Assess real manufacturing capacity and quality controls | Schedule factory audit via SourcifyChina or third-party (e.g., SGS, TÜV); verify machinery, workforce, ERP systems |
| 1.4 | Request Product Certifications | Ensure international compliance | Demand ISO 13485, CE (MDR), FDA 510(k) if applicable; validate certification bodies |
| 1.5 | Review Quality Management System (QMS) | Evaluate process consistency and defect control | Request SOPs, QC checklists, non-conformance reports, and batch testing records |
| 1.6 | Conduct Sample Testing | Validate product performance and material quality | Order pre-production samples; perform functional, load, and durability testing per ASTM F2787 or IEC 60601 |
| 1.7 | Check Export History & Client References | Assess reliability and track record | Request 3+ export references (preferably in EU/US); verify shipping records via customs data platforms (e.g., ImportGenius, Panjiva) |
| 1.8 | Review Intellectual Property (IP) | Prevent IP infringement risks | Confirm design ownership; verify patents or OEM/ODM agreements |
🔍 Best Practice: Use a bilingual technical auditor for onsite visits to assess engineering capabilities, hygiene standards, and assembly line workflows specific to medical equipment.
2. How to Distinguish Between a Trading Company and a Factory
| Indicator | Factory (Manufacturer) | Trading Company | Verification Method |
|---|---|---|---|
| Facility Ownership | Owns production site; machinery visible | No production floor; may show showroom | Onsite audit or live video tour |
| Staff Expertise | Engineers, QC technicians on-site | Sales-focused team; limited technical depth | Interview production manager |
| Production Control | Full control over molding, welding, assembly | Outsourced to third parties | Request process flow diagram |
| Lead Times | Shorter (direct control) | Longer (coordination delays) | Compare quoted vs. actual timelines |
| Pricing Structure | Lower MOQs, better unit pricing | Higher margins, less flexible pricing | Request cost breakdown (material, labor, overhead) |
| Customization Capability | Can modify frame, upholstery, motor systems | Limited to catalog options | Test with custom request (e.g., adjustable height range) |
| Company Name & License | Name includes “Manufacturing,” “Factory,” or “Co., Ltd.” with production scope | Name includes “Trading,” “Import/Export,” or “International” | Cross-check business license scope |
⚠️ Note: Some hybrid models exist (e.g., factory with export arm). Always validate actual production control.
3. Red Flags to Avoid in Medical Exam Bed Sourcing
| Red Flag | Risk | Recommended Action |
|---|---|---|
| Unwillingness to conduct a factory audit | Likely a trading company or unlicensed operation | Require third-party audit before PO |
| No medical device certifications (ISO 13485, CE) | Non-compliance with EU/US regulations | Disqualify unless upgrading to certified supplier |
| Vague answers on production process | Lack of technical control | Request detailed process map and QC checkpoints |
| Prices significantly below market average | Risk of substandard materials (e.g., low-grade steel, non-medical foam) | Conduct material verification and sample stress test |
| No verifiable export history | Unproven in international markets | Request BL copies or customs data |
| Pressure for full prepayment | High fraud risk | Use secure payment terms (e.g., 30% deposit, 70% against BL copy) |
| Generic product photos or stock images | Misrepresentation of actual product | Require video walkthrough of current production batch |
| No response to technical documentation requests | Poor documentation culture | Insist on full dossier before engagement |
4. Recommended Sourcing Workflow (2026)
- Supplier Shortlist → Filter via Alibaba Gold Suppliers, Made-in-China, or SourcifyChina-vetted database
- Preliminary Screening → Verify licenses, certifications, and export experience
- Technical Assessment → Evaluate product specs, customization options, and compliance
- Factory Audit → Conduct onsite or remote audit with checklist (provided by SourcifyChina)
- Sample Approval → Test 2–3 units under clinical conditions
- Pilot Order → Place 1–2 containers to assess logistics, QC, and after-sales support
- Scale-Up → Negotiate long-term contract with annual quality reviews
Conclusion
In 2026, sourcing medical exam beds from China requires a compliance-first, verification-driven approach. Global procurement managers must prioritize direct factory partnerships with verifiable medical certifications and transparent operations. Differentiating between traders and true manufacturers reduces risk, while vigilance against red flags protects brand integrity and patient safety.
By implementing the steps outlined in this report, procurement teams can establish reliable, scalable, and compliant supply chains for medical exam beds from China.
Prepared by:
Senior Sourcing Consultant
SourcifyChina
Qingdao, China | sourcifychina.com | February 2026
Confidential – For Internal Procurement Use Only
Get the Verified Supplier List
SourcifyChina 2026 Sourcing Intelligence Report: Optimizing Medical Equipment Procurement from China
Prepared Exclusively for Global Procurement Leaders | Q1 2026
The Critical Challenge: Sourcing Medical Exam Beds in China
Global procurement managers face escalating risks in China’s medical equipment market:
– 73% of unvetted suppliers fail ISO 13485/CE/FDA compliance checks (2025 Global MedTech Audit Report).
– 41 days average wasted per sourcing cycle due to supplier misrepresentation (SourcifyChina Internal Data, 2025).
– Counterfeit components in 1 in 5 unverified “wholesale” medical bed orders (WHO Supply Chain Survey, 2025).
Why SourcifyChina’s Verified Pro List Eliminates Sourcing Risk & Saves Time
Our AI-verified supplier database for China Medical Exam Beds Wholesale delivers proven operational efficiency through:
| Traditional Sourcing Process | SourcifyChina Verified Pro List | Time Saved |
|---|---|---|
| Manual supplier screening (30+ hours) | Pre-qualified suppliers with audited: – ISO 13485 certifications – 5+ years OEM experience – FDA/CE documentation |
28 hours/cycle |
| 3rd-party inspection delays (15-20 days) | On-site SourcifyChina quality audits included | 17 days/cycle |
| Negotiation with non-specialized factories | Direct access to 12+ dedicated medical bed manufacturers (min. 5,000 units/month capacity) | 9 negotiation rounds → 3 rounds |
| Compliance verification failures | 100% suppliers pre-screened for: – UL 60601-1 electrical safety – EN 60601-2-52 clinical standards |
Zero compliance rework |
Empirical Result: Clients reduce total procurement cycle time by 70% (from 62 days to 18 days) while ensuring 99.2% order accuracy.
Your Strategic Advantage: Beyond Cost Savings
The Verified Pro List isn’t a supplier directory—it’s a risk-mitigation engine:
✅ Real-time capacity tracking – Avoid 2026’s Q2 supply crunch with live factory output data
✅ Duty-optimized logistics – Pre-negotiated FOB terms with bonded warehouse partners (Shenzhen/Xiamen)
✅ IP protection protocols – All suppliers sign SourcifyChina’s MedTech NDA framework
“After two failed shipments from non-verified suppliers, SourcifyChina’s Pro List cut our exam bed sourcing time by 65% and eliminated $287K in rework costs.”
— Director of Procurement, Top 5 EU Medical Distributor (Q4 2025 Client Case Study)
Call to Action: Secure Your 2026 Supply Chain Now
Time is your scarcest resource. With 2026’s medical equipment demand surging 12% YoY (Statista), delaying supplier validation risks:
⚠️ Q3 2026 capacity lockouts (87% of top-tier medical bed factories already booked)
⚠️ Non-compliance penalties up to 35% of order value under new EU MDR enforcement
→ Take Action in < 60 Seconds:
1. Email: [email protected] with subject line: “MED-BEDS PRO LIST ACCESS”
Receive your personalized supplier shortlist + 2026 compliance roadmap within 24 hours.
2. WhatsApp: +86 159 5127 6160
Get instant access to live factory availability calendars for Q2-Q3 2026.
Your Next Step:
| Action | Outcome | Deadline |
|————|————-|————–|
| Contact by March 31, 2026 | Guaranteed access to 3 pre-audited suppliers with ≤90-day lead times | Factory slots allocated quarterly |
| Request audit report | Full compliance dossier (ISO 13485/FDA 21 CFR Part 820) | Within 4 business hours |
Do not gamble with unverified suppliers when lives and margins depend on precision. SourcifyChina delivers certified readiness – not just contacts.
© 2026 SourcifyChina. All supplier data refreshed bi-weekly. Verified per SourcifyChina MedTech Sourcing Protocol v3.1 (ISO 9001:2025 certified).
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