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Pentair

FDA UDI

Class II (US FDA UDI)

by Pentair Filtration Solutions

Identity

Trade Name
Pentair FDA UDI
Generic Name
Non-respiratory device ambient air filter FDA UDI
Model / Reference
100662920 FDA UDI

Identifiers

Catalog Number
DBF32K04-O FDA UDI
Primary DI / UDI-DI
B4621006629203 FDA UDI
510(k) Number
K061426 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Non-respiratory device ambient air filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-respiratory device ambient air filter

Pentair by Pentair Filtration Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-respiratory device ambient air filter.

Cleared under the same submission

K061426 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pentair Filtration Solutions

Sources (1)

  • FDA UDI 39c962b6-5d78-4157-9bfa-ff6e2b50c6d0 36 fields · synced May 30, 2026