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Somnera Airbox Air Filter Pack

FDA UDI

Class II (US FDA UDI)

by Fresca Medical, Inc.

Identity

Trade Name
Somnera Airbox Air Filter Pack FDA UDI
Generic Name
CPAP/BPAP unit ambient air filter, reusable FDA UDI
Device Name
Air Filter pack for use with Somnera Airbox Flow Generator FDA UDI
Model / Reference
19423 FDA UDI
Description
Air Filter pack for use with Somnera Airbox Flow Generator FDA UDI

Identifiers

Catalog Number
19423 FDA UDI
Primary DI / UDI-DI
30810045450132 FDA UDI
510(k) Number
K200698 FDA UDI
FDA Product Code
QBY FDA UDI
GMDN Term
CPAP/BPAP unit ambient air filter, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5273 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: CPAP/BPAP unit ambient air filter, reusable

Somnera Airbox Air Filter Pack by Fresca Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP unit ambient air filter, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7222606-8ff8-4e21-a412-11aef54ad82f 37 fields · synced Jun 1, 2026