← Back to catalogue

Veraseal 3 Full Face Vented Mask, Small

FDA UDI

Class II (US FDA UDI)

by Sleepnet Corporation

Identity

Trade Name
Veraseal 3 Full Face Vented Mask, Small FDA UDI
Generic Name
CPAP/BPAP face mask, single-use FDA UDI
Device Name
Disposable full face vented mask for use in positive pressure ventilation. FDA UDI
Model / Reference
50843 FDA UDI
Description
Disposable full face vented mask for use in positive pressure ventilation. FDA UDI

Identifiers

Primary DI / UDI-DI
00814747021453 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP face mask, single-use 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: CPAP/BPAP face mask, single-use

Veraseal 3 Full Face Vented Mask, Small by Sleepnet Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sleepnet Corporation

Sources (1)

  • FDA UDI 88702ca0-1304-497c-aaa2-a3c4f63f285e 35 fields · synced Jun 9, 2026