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T.l.i.f. Sg Instruments
EUDAMEDFDA UDIClass I (EU MDR)
Ref 202711107Model TLIF SG Spoons and Curettes
Identity
- Trade Name
- T.L.I.F. SG INSTRUMENTS EUDAMEDT.L.I.F. FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Curette EUDAMEDT.L.I.F. SG INSTRUMENTS RING CURETTE, ANGLED FDA UDI
- Model / Reference
- TLIF SG Spoons and Curettes EUDAMED202711107 EUDAMEDFDA UDI
- Description
- T.L.I.F. SG INSTRUMENTS RING CURETTE, ANGLED FDA UDI
Identifiers
- Catalog Number
- 202711107 FDA UDI
- Primary DI / UDI-DI
- 10705034184296 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a000745Z EUDAMED
- Direct Marketing DI
- 10705034184296 EUDAMED
- FDA Product Code
- HTF FDA UDI
- EMDN Code
- L0901 ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE EUDAMED
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone curette, reusable
T.l.i.f. Sg Instruments by Medos International Sarl — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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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 | 0705034a000745Z | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Medos International SARL
- EUDAMED SRN
- CH-MF-000014268
- Authorised Representative
- DePuy Ireland UC IE-AR-000009328
Sources (2)
- EUDAMED eb1dc73e-b00e-4c0a-9f70-1fa37829af9e 61 fields · synced Jun 17, 2026
- FDA UDI d9ee0ae3-a416-4500-885c-7482991d8eb4 35 fields · synced May 29, 2026