Identity
- Trade Name
- COVAORTHO-NERVE FDA UDI
- Generic Name
- Surgical anti-adhesion material, implantable, bioabsorbable, non-medicated FDA UDI
- Device Name
- Collagen Guided Healing Membrane FDA UDI
- Model / Reference
- MCG 12 23 V FDA UDI
- Description
- Collagen Guided Healing Membrane FDA UDI
Identifiers
- Catalog Number
- COVO23 FDA UDI
- Primary DI / UDI-DI
- 03760193182026 FDA UDI
- 510(k) Number
- K103081 FDA UDI
- FDA Product Code
- JXI FDA UDI
- GMDN Term
- Surgical anti-adhesion material, implantable, bioabsorbable, non-medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5275 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 30 Millimeter FDA UDIWidth — 20 Millimeter FDA UDI
Covaortho-Nerve by Dilon Technologies France — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Dilon Technologies France
Sources (1)
- FDA UDI 5b97cc7a-7290-4122-b690-cf5c183640f3 39 fields · synced Jun 6, 2026