← Back to catalogue
Pituitary Rongeur Str
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2305-10-000
by Tecomet, Inc
Identity
- Trade Name
- PITUITARY RONGEUR STR EUDAMEDTecomet FDA UDI
- Generic Name
- Orthopaedic joint/limb rongeur FDA UDI
- Device Name
- Rongeurs EUDAMEDPITUITARY RONGEUR STR FDA UDI
- Model / Reference
- 2305-10-000 EUDAMEDFDA UDI
- Description
- PITUITARY RONGEUR STR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841435120778 EUDAMEDFDA UDI
- Basic UDI-DI
- 0841435132853U5 EUDAMED
- Direct Marketing DI
- 00841435120778 EUDAMED
- FDA Product Code
- HTX FDA UDI
- EMDN Code
- L091307 ORTHOPAEDIC SURGERY RONGEURS, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic joint/limb rongeur FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Belgium 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
Pituitary Rongeur Str by Tecomet, Inc — 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 | 0841435132853U5 | 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
- Tecomet, Inc
- EUDAMED SRN
- US-MF-000027544
- Authorised Representative
- Meditec Source GmbH & Co. KG DE-AR-000009318
Sources (2)
- EUDAMED 4ce24fd8-a5e9-4b01-b97f-01d80b4debf7 61 fields · synced Sep 17, 2026
- FDA UDI adbd7b3d-7522-428b-a069-8a07ae2649ee 33 fields · synced May 29, 2026