Atramat PGC25
by Internacional Farmacéutica S.A DE C.V 64 variants
Atramat PGC25 (HPE1904-B) is a Class II device made by Internacional Farmacéutica S.A DE C.V, cleared under FDA 510(k) K072863 on 23 May 2008 and listed in FDA GUDID since 11 Jul 2018 (UDI-DI 07500142057038), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07500142057038 | Date11 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK072863 | Date23 May 2008 | StatusActive |
Official records
- AccessGUDID record 07500142057038
- FDA 510(k) database K072863
Across registries
- FDA 510(k) K072863 decided 23 May 2008 Active
- FDA GUDID UDI-DI 07500142057038 listed 11 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K072863
- Listed FDA GUDID 07500142057038
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Atramat
- Generic name
- Poliglecaprone suture
- Model / Ref / Catalog
- PGC25, HPE1904-B
- Primary DI / UDI-DI
- 07500142057038
- 510(k) Number
- FDA product code
- GAM
- GMDN term
- Poliglecaprone suture
- Device class
- Class II
- Regulation number
- 878.4493
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 19 Millimeter
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