LAB
Testing Laboratory · Germany
Match: 94/100ISO/IEC 17025 accredited lab offering EN 60601 electrical safety testing and ISO 10993 biocompatibility assessment for Class IIa medical devices.
EN 60601ISO 10993MDR
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Platform preview
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Hi! Tell me about your product and what you need — I'll turn it into a structured request.
👤
Class IIa surgical instrument, need EN 60601 testing plus ISO 10993 biocompatibility. We're based in Germany.
Got it. Do you already have a technical file, or should the lab start from a specification review?
👤
I have a draft — I can attach it.
Perfect — your request is ready. Sending it to 3 matching labs now.
Application Draft
TESTING LAB (LAB)
4 / 4 fields collected
Product
Class IIa surgical instrument
Testing needed
EN 60601, ISO 10993 biocompatibility
Location
Germany
Documentation
Draft technical file available
✅ All required fields collected!
| Application | Status / Action | AI Score | Submitted | Providers | Provider Response |
|---|---|---|---|---|---|
|
Industrial Robot Arm IR-500
Notified Body
|
Approved |
87%
HIGH
|
15 Mar 2026 | 3 |
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After unlock — full access
LAB
MedTech Prüflabor GmbH
Testing Laboratory · Germany Match: 94/100ISO/IEC 17025 accredited lab offering EN 60601 electrical safety testing and ISO 10993 biocompatibility assessment for Class IIa medical devices.
EN 60601ISO 10993MDR
✅
contact@medtech-lab.de · +49 30 1234 5678 · www.medtech-lab.de
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Pricing
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Get 12-Month AccessThe problem
Three ways to find a compliance provider. All of them broken.
1. The official registries
NANDO lists Notified Bodies — but only Notified Bodies. No labs, no authorised representatives, no consultants. No way to know who responds to emails, covers your product category, or takes new clients.
You get an official list, but not an answer.
2. The Google search
Page after page of provider websites that don't say what they actually do. You send twenty emails, get five replies, and find out three weeks later that the lab doesn't cover your directive.
You save money upfront, but pay in weeks and dead ends.
3. The consultant
A regulatory consultant will build you a provider shortlist — at €150–300 per hour. Solid work, and valuable for regulatory strategy — but provider discovery alone doesn't need expert hourly rates.
You get the answer, but at fifty times the cost.
Or: one platform. 13,500+ providers, one AI-drafted request that reaches every match. From €120/6 months.
The data
What's in ECP
13,500+providers across the EU and EEA
of which
12languages: English, Deutsch, Polski, Français, Español, Italiano, Čeština, Türkçe, Українська, Русский, 中文, 日本語
35+EU regulations and directives covered
27EU member states + EEA
Explorer
Understand the rules before you choose a partner
Free guides and articles on EU regulations, certification routes and market access — from MDR timelines to GPSR obligations. Written for manufacturers, not lawyers.
MDR
Browse all guides →
MDR certification timelines in 2026
Which Notified Bodies have capacity — current queue times, realistic durations and how to prepare.
GPSRGPSR obligations for non-EU sellers
Who needs a responsible economic operator and what the regulation actually requires.
CE MarkingCE marking routes explained
Step by step from product classification and conformity assessment to the Declaration of Conformity.
FAQ
Questions, answered
How does the free search work?
No account, no credit card. Describe your product and regulation — the AI assistant shows real matched providers with their type, country, capabilities and match quality. Search as many times as you need. Provider names and contact details stay blurred until you unlock full access.
What exactly do I get with a subscription?
Full access to all 13,500+ provider profiles: direct contact details, services, regulations covered and countries, unlimited AI-assisted searches, and an AI-drafted request sent to every provider you select, with replies arriving in your cabinet. 6- or 12-month access, renewed manually — no automatic billing, no per-search fees.
How do I contact the providers I find?
Two ways. Use their unlocked direct contacts — email, phone, website. Or let the platform do the work: select providers in the results, and the AI assistant will prepare a structured application and send it to all of them at once. Replies and statuses live in your cabinet. Both ways are included in your subscription — no extra fees, no commission.
Which provider types are covered?
Five types: Notified Bodies, testing laboratories, EU Authorised Representatives, certification bodies and regulatory consultants — across all EU member states and the EEA.
Which regulations are covered?
MDR, IVDR, CE marking, GPSR, RED, EMC, LVD, REACH, RoHS, Machinery, PED, CPR, ATEX and other EU regulations and directives — 35+ in total. If your product needs EU market access, the relevant providers are here.
How current is the data?
Profiles are compiled from official EU registries, public records and provider disclosures, and updated continuously. Your subscription includes all updates for as long as it's active.
What if I don't find the right provider?
Search first — free, without limits. You'll see the quality of matches before paying anything. If your case is unusual, contact us and we'll check coverage for your regulation before you buy.
Do you take a commission or represent any providers?
No. We don't sell services, take commissions or promote anyone. Rankings are neutral — you see providers ranked by relevance to your request, nothing else.
What happens when my subscription ends?
Your 6- or 12-month access renews manually — there's no automatic charge. If it lapses, you get a 3-day grace period with full access, and you can renew any time from your cabinet to pick up right where you left off.