Dermapac, Inc. 6080
Dermapac, Inc. 6080 is a Class I device made by Dermapac Inc., listed in FDA GUDID since 12 Sep 2022 (UDI-DI 10810102270747), 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 | Number10810102270747 | Date12 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10810102270747
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dermapac, Inc.
- Generic name
- General-purpose surgical sponge
- Model / reference
- 6080
- Primary DI / UDI-DI
- 10810102270747
- FDA product code
- NAB
- GMDN term
- General-purpose surgical sponge
- Device class
- Class I
- Regulation number
- 878.4014
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code NAB (Gauze / Sponge,Nonresorbable For External Use).
- BONE-DRI SURGICAL SPONGE by Howmedica Corp.
- BANDAGE ROLL, GAUZE by Keilei Intl., Inc.
- CLINISORB by Hermitage Hospital Products, Inc.
- SOF-ROL CAST PADDING by Stan-Pak Ent.
- TRIANGULAR BANDAGE by Abco Dealers, Inc.
- K-BAND AND K-CREPE by Parema, Ltd.
- TRICOTEX WOUND CONTACT LAYER DRESSING by Smith & Nephew, Inc.
- GAUZE SPONGE, STERILE 2'S by Keilei Intl., Inc.
- GAUZE BANDAGE 1 X 6 YDS. by North Health Care
- PDI SURGICAL SCRUB/BRUSH T150-70 by Nice-Pak Products, LLC