Dermapac, Inc. 6016
Dermapac, Inc. 6016 is a Class I device made by Dermapac Inc., listed in FDA GUDID since 12 Sep 2022 (UDI-DI 10810102270594), 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 | Number10810102270594 | Date12 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10810102270594
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- Withdrawn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
- 6016
- Primary DI / UDI-DI
- 10810102270594
- 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).
- ADVANCE LAPAROTOMY SPONGE, LAP SPONGE by Advance Medical Designs, Inc.
- STERILE TONSIL SPONGES by Medspec Corp.
- LAP SPONGES, MODIFIED by Carwild Corp.
- ISOLYSER (8X4 12 PLY X-RAY DETECTABLE) by Thantex Specialties, Inc.
- Symmetry SECTO® 81-1010 by Aspen Surgical Products, Inc.
- PROTEC X-RAY DETECTABLE GAUZE SPONGE by Derivados DE Gasa, S.A. DE C.V.
- SURGICAL SPONGE X-RAY DETECTABLE by MCNEIL HEALTHCARE LLC
- ISOLYSER (18X18 X-RAY DETECTABLE) by Thantex Specialties, Inc.
- TONSIL SPONGE, X-RAY DETECTABLE, W/STRING by BIOSEAL
- GAUZE PACKING, X-RAY DETECTABLE by BIOSEAL