Dermapac, Inc. 6003
Dermapac, Inc. 6003 is a Class I device made by Dermapac Inc., listed in FDA GUDID since 12 Sep 2022 (UDI-DI 10810102270549), 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 | Number10810102270549 | Date12 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10810102270549
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- Withdrawn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
- 6003
- Primary DI / UDI-DI
- 10810102270549
- 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).
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- LORREX GAUZE SPONGES, X-RAY DETECTABLE by Lorrex Health Products
- GAUZE & COTTON SPONGES by Medtech Intl., Inc.
- ROUND STICK SPONGES, FLAT STICK SPONGES by Medical Perspectives Corp.
- GAUZE SPONGE, X-RAY DETECTABLE by Bioseal, Inc.
- LAP SPONGE PRODUCT LINE by Cush Medical Products
- X-RAY DETECTABLE BAND by Isramed, Inc.