Identity
- Trade Name
- S+N ORD - Zimmer EUDAMEDFDA UDI
- Generic Name
- Surgical power tool adaptor FDA UDI
- Device Name
- Reamer Drivers and Acetabular Reamers EUDAMEDA surgical instrument connected to an active device intended to be used during an orthopaedic surgical procedure FDA UDI
- Model / Reference
- 4250-7410 EUDAMEDFDA UDI
- Description
- A surgical instrument connected to an active device intended to be used during an orthopaedic surgical procedure FDA UDI
Identifiers
- Catalog Number
- 4250-7410 FDA UDI
- Primary DI / UDI-DI
- 09421038410103 EUDAMEDFDA UDI
- Basic UDI-DI
- 942102811GMN003022 EUDAMED
- Direct Marketing DI
- 09421028113274 EUDAMED
- FDA Product Code
- HWE FDA UDI
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Surgical power tool adaptor FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Market of Registration
- Netherlands 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
No
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
S+N ORD - Zimmer by Enztec Limited — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 942102811GMN003022 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Enztec Limited
- EUDAMED SRN
- NZ-MF-000002264
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 92321bc7-2375-45d4-b511-a242ef2ef9e6 61 fields · synced Jun 17, 2026
- FDA UDI 98d05307-6fa2-4ef1-a834-89f4f9b5ed6c 34 fields · synced May 30, 2026