Dermapac, Inc. 5010
Dermapac, Inc. 5010 is a Class I device made by Dermapac Inc., listed in FDA GUDID since 12 Sep 2022 (UDI-DI 10810102270259), 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 | Number10810102270259 | Date12 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10810102270259
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- Withdrawn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
- 5010
- Primary DI / UDI-DI
- 10810102270259
- 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).
- CHERRY PIT DISSECTOR by Medical Perspectives Corp.
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- GAUZE SPONGE by South Mountain Medical
- ISOLYSER (4X18) X-RAY DETECTABLE by Thantex Specialties, Inc.
- KENSORB by KENTRON HEALTH CARE, INC.
- NEUROSPONGE PADDIE by Winn Hirsch & Assoc.
- SIMPEX INC. SURGICAL DRESSING by Simpex, Inc.
- POLYESTER X-RAY DETECTABLE STRUNG-SPONGE by American Medical Disposable, Inc.
- COTTON BALLS, X-RAY OPAQUED STRUNG & NON by American Medical Disposable, Inc.
- X-RAY DETECTABLE GAUZE SPONGE by Keilei Intl., Inc.