Screwdriver EUROSCREW NG
EUDAMEDFDA UDIClass I (EU MDR)
by Teknimed Sas
Identity
- Trade Name
- Screwdriver EUROSCREW NG EUDAMEDEUROSCREW NG screwdriver FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Model / Reference
- Reusable Surgical Instruments EUDAMEDT067231 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760177042421 EUDAMEDFDA UDI
- Basic UDI-DI
- 376017704B27DC EUDAMED
- Direct Marketing DI
- 03760177042421 EUDAMED
- FDA Product Code
- HXX FDA UDI
- EMDN Code
- L091099 OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Surgical implant template, reusable
Screwdriver EUROSCREW NG by Teknimed Sas — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 376017704B27DC | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Teknimed Sas
- EUDAMED SRN
- FR-MF-000001224
Sources (2)
- EUDAMED e2e67ef9-abcb-4b0c-934f-72dbf6a4099c 61 fields · synced Jul 9, 2026
- FDA UDI efce3110-46e5-49bb-ac00-36a7c0254ff8 32 fields · synced May 30, 2026