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CPAP Chinstrap

FDA UDI

Class I (US FDA UDI)

by Pepper Medical, Inc.

Identity

Trade Name
CPAP Chinstrap FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Device Name
CPAP Chinstrap FDA UDI
Model / Reference
AA-09 FDA UDI
Description
CPAP Chinstrap FDA UDI

Identifiers

Catalog Number
AA-09 FDA UDI
Primary DI / UDI-DI
10850014574786 FDA UDI
FDA Product Code
BTK FDA UDI
GMDN Term
CPAP/BPAP nasal mask, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5560 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
MRI Safety
MR Safe FDA UDI

Category: CPAP/BPAP nasal mask, reusable

CPAP Chinstrap by Pepper Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP nasal mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20ce367a-ecab-4598-af11-6316d10373a2 35 fields · synced Jun 8, 2026