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Endo-Flexprobe, standard
EUDAMEDFDA UDIClass I (EU MDR)
Ref TEFP32020
by Joimax GmbH
Identity
- Trade Name
- Endo-Flexprobe, standard EUDAMEDprobe FDA UDI
- Generic Name
- Nerve/vessel retractor FDA UDI
- Device Name
- Endo-Flexprobe EUDAMEDEndo-Flexprobe, standard EUDAMEDFDA UDI
- Model / Reference
- TEFP32020 EUDAMEDFDA UDI
- Description
- Endo-Flexprobe, standard FDA UDI
Identifiers
- Catalog Number
- TEFP32020 FDA UDI
- Primary DI / UDI-DI
- 04250337101208 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371PALPENDG5 EUDAMEDB-04250337101208 EUDAMED
- FDA Product Code
- GEG FDA UDI
- EMDN Code
- L031102 EXPLORATION PROBES, REUSABLE EUDAMED
- GMDN Term
- Nerve/vessel retractor FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Endo-Flexprobe, standard by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 42503371PALPENDG5 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 42503371PALPENDG5 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Joimax GmbH
- EUDAMED SRN
- DE-MF-000009201
Sources (3)
- EUDAMED 553759d9-cf4b-4141-8a4e-322d4c1918d3 61 fields · synced Jul 11, 2026
- EUDAMED 88b42f93-3f58-44e8-a340-5aaf60390829 61 fields · synced May 16, 2026
- FDA UDI ba7b0ec5-e06d-4837-9739-eb7ca302f57d 36 fields · synced May 30, 2026