Dukal 879
by Dukal LLC
Dukal 879 is a Class I device made by Dukal LLC, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 00665973010182), registry data as of 22 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 | Number00665973010182 | Date6 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 00665973010182
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dukal
- Generic name
- General-body orifice lubricant
- Model / Ref / Catalog
- 879
- Primary DI / UDI-DI
- 00665973010182
- FDA product code
- KMJ
- GMDN term
- General-body orifice lubricant
- Device class
- Class I
- Regulation number
- 880.6375
- GUDID distribution status
- In Commercial Distribution
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