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Amara View

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Amara View FDA UDI
Generic Name
CPAP/BPAP face mask, reusable FDA UDI
Device Name
mask cushion FDA UDI
Model / Reference
00 FDA UDI
Description
mask cushion FDA UDI

Identifiers

Catalog Number
1090692 FDA UDI
Primary DI / UDI-DI
00606959009332 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP face mask, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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 face mask, reusable

Amara View by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP face mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 623666b6-47fd-4c5f-9eed-978a86e0ee1f 36 fields · synced Jun 8, 2026