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Conduit Tlif
EUDAMEDFDA UDIClass I (EU MDR)
Ref PEC00103CModel Conduit Cases and Trays for Spinal Medical Devices
Identity
- Trade Name
- CONDUIT TLIF EUDAMEDCONDUIT FDA UDI
- Generic Name
- Surgical instrument/implant rack FDA UDI
- Device Name
- Conduit Cases and Trays for Spinal Medical Devices EUDAMEDCONDUIT TLIF Core Instrument Tray FDA UDI
- Model / Reference
- Conduit Cases and Trays for Spinal Medical Devices EUDAMEDPEC00103C EUDAMEDFDA UDI
- Description
- CONDUIT TLIF Core Instrument Tray FDA UDI
Identifiers
- Catalog Number
- PEC00103C FDA UDI
- Primary DI / UDI-DI
- 10705034569475 EUDAMEDFDA UDI
- Basic UDI-DI
- 0705034a000415J EUDAMED
- Direct Marketing DI
- 10705034569475 EUDAMED
- FDA Product Code
- FSM FDA UDI
- EMDN Code
- V0499 CLINICAL USE CONTAINERS (NON-IVD) - OTHER EUDAMED
- GMDN Term
- Surgical instrument/implant rack 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
No
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: Instrument transport trolley system
Conduit Tlif 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 | 0705034a000415J | 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 2131a203-616f-4503-9cd8-f6b9f70d8f5a 61 fields · synced Jul 11, 2026
- FDA UDI 80515696-2284-4fe3-af8d-7486255af4ac 35 fields · synced May 30, 2026