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Ascend Nasal Airgel Cushion Medium

FDA UDI

Class II (US FDA UDI)

by Sleepnet Corporation

Identity

Trade Name
Ascend Nasal Airgel Cushion Medium FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Device Name
Replacement cushion for nasal vented mask used with positive pressure ventilation. FDA UDI
Model / Reference
50202 FDA UDI
Description
Replacement cushion for nasal vented mask used with positive pressure ventilation. FDA UDI

Identifiers

Primary DI / UDI-DI
00814747020258 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP nasal 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: CPAP/BPAP nasal mask, reusable

Ascend Nasal Airgel Cushion Medium by Sleepnet Corporation — Class II — 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

Manufacturer
Sleepnet Corporation

Sources (1)

  • FDA UDI e30c438a-c4e1-470d-b4a8-41ca800af832 34 fields · synced Jun 9, 2026