Contract manufacturerPentair Filtration Solutions (Saint Paul, MN)MinnesotaAnesthesiologyClass II
Pentair Filtration Solutions
Contract manufacturer · Saint Paul, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2132517 (openFDA record; or search FDA's registration database)
- FEI number
- 1000221012
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Pentair Filtration Solutions (FDA owner/operator no. 9009435)
- Registered address
- 1350 Hammond Rd, Saint Paul, MN 55110
- Contract listings
- 1 device listings, 1 product codes, first listed Mar 4, 2016
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| CAH | Filter, Bacterial, Breathing-Circuit | Class II | Anesthesiology | Contract manufacturing | Mar 4, 2016 |