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Apex

FDA UDI

Class II (US FDA UDI)

by Wellell Inc.

Identity

Trade Name
APEX FDA UDI
Generic Name
Alternating-pressure chair cushion, reusable FDA UDI
Device Name
9P-077520 Domus Auto FDA UDI
Model / Reference
9P-077520 FDA UDI
Description
9P-077520 Domus Auto FDA UDI

Identifiers

Primary DI / UDI-DI
04713025002435 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure chair cushion, reusable 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alternating-pressure chair cushion, reusable

Apex by Wellell Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure chair cushion, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wellell Inc.

Sources (1)

  • FDA UDI f0b6b55d-d9a1-44fd-a87e-03db72027a4a 33 fields · synced May 30, 2026