Parietex PCO2015FX
Parietex PCO2015FX is a Class II device made by Sofradim Production, listed in FDA GUDID since 6 Oct 2015 (UDI-DI 10884521179752), 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 | Number10884521179752 | Date6 Oct 2015 | StatusListed |
Official records
- AccessGUDID record 10884521179752
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Parietex
- Generic name
- Extra-gynaecological surgical mesh, composite-polymer
- Model / reference
- PCO2015FX
- Primary DI / UDI-DI
- 10884521179752
- FDA product code
- FTL
- GMDN term
- Extra-gynaecological surgical mesh, composite-polymer
- Device class
- Class II
- Regulation number
- 878.3300
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 20 CentimeterWidth — 15 Centimeter
Similar devices in this category
Other devices filed under Extra-gynaecological surgical mesh, composite-polymer.
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- Biomesh® CA.B.S.’Air® Composite CABSAIRC7 by Cousin Biotech Sas
- Parietex PCOPM15H50 by SOFRADIM PRODUCTION
- Parietex PCO4VP by SOFRADIM PRODUCTION