Strattice Reconstructive Tissue Matrix 0610008
Strattice Reconstructive Tissue Matrix 0610008 is a Class II device made by Lifecell Corp, listed in FDA GUDID since 17 Sep 2015 (UDI-DI M32806100080), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM32806100080 | Date17 Sep 2015 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Strattice Reconstructive Tissue Matrix
- Generic name
- Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial
- Model / Ref / Catalog
- 0610008
- Primary DI / UDI-DI
- M32806100080
- FDA product code
- FTM
- GMDN term
- Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.3300
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 10 CentimeterLength — 6 Centimeter
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