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Bacteria Filter

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Bacteria Filter FDA UDI
Generic Name
Respirator filter/cartridge, particulates FDA UDI
Device Name
CPAP Final Bacteria Filters 10/Pack FDA UDI
Model / Reference
APAR008BF2200-10 FDA UDI
Description
CPAP Final Bacteria Filters 10/Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00848530083571 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Respirator filter/cartridge, particulates 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Respirator filter/cartridge, particulates

Bacteria Filter by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respirator filter/cartridge, particulates.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c668d9f3-aa67-4be0-8c67-06c6bac7eb74 34 fields · synced Jun 7, 2026