Dukal 6125
by Dukal LLC
Dukal 6125 is a Class I device made by Dukal LLC, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 10665973014835), 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 | Number10665973014835 | Date6 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 10665973014835
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dukal
- Generic name
- Non-woven gauze pad
- Model / Ref / Catalog
- 6125
- Primary DI / UDI-DI
- 10665973014835
- FDA product code
- NAB
- GMDN term
- Non-woven gauze pad
- Device class
- Class I
- Regulation number
- 878.4014
- GUDID distribution status
- In Commercial Distribution
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