Dermapac, Inc. 5709
Dermapac, Inc. 5709 is a Class I device made by Dermapac Inc., listed in FDA GUDID since 12 Sep 2022 (UDI-DI 10810102270495), 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 | Number10810102270495 | Date12 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10810102270495
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dermapac, Inc.
- Generic name
- Radiopaque woven surgical sponge
- Model / reference
- 5709
- Primary DI / UDI-DI
- 10810102270495
- FDA product code
- GDY
- GMDN term
- Radiopaque woven surgical sponge
- Device class
- Class I
- Regulation number
- 878.4450
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code GDY (Gauze/Sponge, Internal, X-Ray Detectable).
- TRIANGULAR SPONGES by Medical Perspectives Corp.
- LAPAROTOMY SPONGES by American Healthcare, Inc.
- TOMAC STERILE DISP. LAP SPONGE by American Convertors Div., American Pharmaseal
- SPONGE, LAPAROTOMY, VARIOUS SIZE by Shawnee Products, Inc.
- Symmetry SECTO® 81-1000 by Aspen Surgical Products, Inc.
- Expanding ear tampon 66410 by Spiggle & Theis Medizintechnik GmbH
- Symmetry SECTO® 81-1012 by Aspen Surgical Products, Inc.
- TENCEL X-RAY DETECTABLE SPONGES/LAP PADS by Courtaulds Fibers, Inc.
- X-RAY DETECTABLE COTTON BALLS by American Silk Sutures, Inc.
- SPONGES, STANFORD STERILE LAP by Stanford Professional Products