← Back to catalogue
Trial Plug Ø16mm
EUDAMEDFDA UDIClass I (EU MDR)
Ref T067706Model Reusable Surgical Instruments
by Teknimed Sas
Identity
- Trade Name
- Trial Plug Ø16mm EUDAMEDCEMSTOP INSTRUMENTATION FDA UDI
- Generic Name
- Orthopaedic cement restrictor sizer FDA UDI
- Model / Reference
- Reusable Surgical Instruments EUDAMEDT067706 EUDAMEDTrial plug DIAMETER 16 mm FDA UDI
Identifiers
- Catalog Number
- T067706 FDA UDI
- Primary DI / UDI-DI
- 03760177040298 EUDAMEDFDA UDI
- Basic UDI-DI
- 376017704B27DC EUDAMED
- Direct Marketing DI
- 03760177040298 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Orthopaedic cement restrictor sizer 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Trial Plug Ø16mm by Teknimed Sas — Class I — 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 | 376017704B27DC | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Teknimed Sas
- EUDAMED SRN
- FR-MF-000001224
Sources (2)
- EUDAMED 194f161b-2c75-4abe-9d99-c4064ec67014 61 fields · synced Jun 18, 2026
- FDA UDI cd9e3588-f3b6-4fc7-b96b-6c062f55651f 33 fields · synced May 30, 2026