FDA Registration
Active
🇺🇸 United States
Pentair Filtration Solutions
Reg #: 2132517
·
FEI: 1000221012
·
Expires 2026
Products
3
Proprietary Names
8
Establishment Types
2
Classifications
3
Registration Details
- Registration Name
- Pentair Filtration Solutions
- Registration Number
- 2132517
- FEI Number
- 1000221012
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 1350 Hammond Rd
- City
- Saint Paul
- State
- MN
- ZIP
- 55110
- Country
- US
Regulatory Submissions
- 510(k) Number
- K061426
Owner / Operator
- Firm Name
- Pentair Filtration Solutions
- Operator Number
- 9009435
- Address
- 1350 HAMMOND RD., --
- City
- Saint Paul
- State
- MN
- Postal Code
- 55110
- Country
- US
- Correspondent
- Roger A Hanzalik
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Filter, Bacterial, Breathing-Circuit | CAH | Class 2 | Anesthesiology | No | 2007-12-20 |
| Filter, Prebypass, Cardiopulmonary Bypass | KRJ | Class 2 | Cardiovascular | No | 2007-12-20 |
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | Class 2 | Anesthesiology | No | 2006-12-07 |
Proprietary Names
DBF32, DBF24, DBF27,DBF25, DFC06, D
DPB30 Disposable Pre-Bypass Filter
DBF23 DISPOSABLE RESPIRATORY FILTER
DPC20 Disposable Pre-Bypass Filter
HUMIDIFLOW
DBF23 Disposble Main Flow Filter
DBF23 Reuseable Respiratory Filter
DBF23-R Reuseable Main Flow Filter
Establishment Types
Manufacture Medical Device
Manufacture Medical Device for Another Party (Contract Manufacturer)