← Back to catalogue

AtmosAir Velaris

FDA UDI

Class II (US FDA UDI)

by Arjohuntleigh, Inc.

Identity

Trade Name
AtmosAir Velaris FDA UDI
Generic Name
Alternating-pressure bed mattress overlay system FDA UDI
Device Name
AtmosAir VelarisS Mattress - Stretcher -762 x 1910 x 130 mm (30 x 75 x 5 in) - Top Cover Reliant FDA UDI
Model / Reference
633046 FDA UDI
Description
AtmosAir VelarisS Mattress - Stretcher -762 x 1910 x 130 mm (30 x 75 x 5 in) - Top Cover Reliant FDA UDI

Identifiers

Primary DI / UDI-DI
05059441150169 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure bed mattress overlay system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 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

Yes

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

Yes

FDA UDI

Category: Alternating-pressure bed mattress overlay system

AtmosAir Velaris by Arjohuntleigh, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress overlay system.

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
Arjohuntleigh, Inc.

Sources (1)

  • FDA UDI 6c53e8e1-a849-45e1-9195-4fef46ef5674 33 fields · synced May 30, 2026