Identity
- Trade Name
- COMPOSIX FDA UDI
- Generic Name
- Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable FDA UDI
- Device Name
- Composix L/P Mesh with PS Echo PS Positioning System, 7.2" x 9.2" (18.4 cm x 23.5 cm), Ellipse FDA UDI
- Model / Reference
- 0144790 FDA UDI
- Description
- Composix L/P Mesh with PS Echo PS Positioning System, 7.2" x 9.2" (18.4 cm x 23.5 cm), Ellipse FDA UDI
Identifiers
- Catalog Number
- 0144790 FDA UDI
- Primary DI / UDI-DI
- 00801741031366 FDA UDI
- FDA Product Code
- FTL FDA UDIOQL FDA UDIGCJ FDA UDI
- GMDN Term
- Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 FDA UDI876.1500 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
- Width — 7.2 Inch FDA UDILength — 9.2 Inch FDA UDI
Composix by Davol Inc. — 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
- Davol Inc.
Sources (1)
- FDA UDI bf54592e-6e4e-4ccc-b7f1-5b00abee8452 37 fields · synced May 31, 2026