Dermapac, Inc. 8035
Dermapac, Inc. 8035 is a Class I device made by Dermapac Inc., listed in FDA GUDID since 12 Sep 2022 (UDI-DI 10810102271096), 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 | Number10810102271096 | Date12 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10810102271096
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dermapac, Inc.
- Generic name
- General surgical procedure kit, non-medicated, single-use
- Model / reference
- 8035
- Primary DI / UDI-DI
- 10810102271096
- FDA product code
- KDC
- GMDN term
- General surgical procedure kit, non-medicated, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
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