CEGA Innovations, Inc.

FDA UDI

Class I (US FDA UDI)

by Cega Innovations, Inc.

Identity

Trade Name: CEGA Innovations, Inc. FDA UDI
Generic Name: Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name: REMUV Single Patient Use (SPU) Air Transfer Mattress with Skin Integrity Pad (Approx. 36" W x 83" L) FDA UDI
Model / Reference: MV800 FDA UDI
Description: REMUV Single Patient Use (SPU) Air Transfer Mattress with Skin Integrity Pad (Approx. 36" W x 83" L) FDA UDI

Identifiers

Catalog Number: MV800 FDA UDI
Primary DI / UDI-DI: 00850001780032 FDA UDI
FDA Product Code: KME FDA UDI
FMR FDA UDI
GMDN Term: Absorbent underpad, non-antimicrobial, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6060 FDA UDI
880.6785 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 36 Inch FDA UDI
Length — 83 Inch FDA UDI

Category: Absorbent underpad, non-antimicrobial, single-use Patient transfer system, manual

CEGA Innovations, Inc. by Cega Innovations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cega Innovations, Inc.

Sources (1)

FDA UDI c8bb932b-6d54-4172-be69-6bfaf6ec4ccf 37 fields · synced May 30, 2026