Pentair 10005336
by Pentair Filtration Solutions
Pentair 10005336 (DBF23K040) is a Class II device made by Pentair Filtration Solutions, listed in FDA GUDID since 21 Aug 2026 (UDI-DI B462100053363), 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 | NumberB462100053363 | Date21 Aug 2026 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pentair
- Generic name
- Non-respiratory device ambient air filter
- Model / Ref / Catalog
- 10005336, DBF23K040
- Primary DI / UDI-DI
- B462100053363
- FDA product code
- CAH
- GMDN term
- Non-respiratory device ambient air filter
- Device class
- Class II
- Regulation number
- 868.5260
- GUDID distribution status
- In Commercial Distribution
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