Identity
- Trade Name
- CONCORDE LIFT FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- CONCORDE LIFT INSTRUMENTS IMPLANT CASE-US FDA UDI
- Model / Reference
- 2878-04-116G FDA UDI
- Description
- CONCORDE LIFT INSTRUMENTS IMPLANT CASE-US FDA UDI
Identifiers
- Catalog Number
- 287804116G FDA UDI
- Primary DI / UDI-DI
- 10705034531328 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Concorde Lift by Medos International Sàrl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI a39c6b34-1e8c-4f47-ac91-e4491bfb3752 36 fields · synced Jun 1, 2026