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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 system FDA UDI
Device Name
Sedens 400 FDA UDI
Model / Reference
9P-087000 FDA UDI
Description
Sedens 400 FDA UDI

Identifiers

Primary DI / UDI-DI
04719893348781 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure chair cushion 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alternating-pressure chair cushion system

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 system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wellell Inc.

Sources (1)

  • FDA UDI 4b67fc75-38ab-4b36-9ebd-63a01ced5dad 33 fields · synced May 30, 2026