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Prevena™ Customizable™

FDA UDI

Class II (US FDA UDI)

by Kci Usa, Inc.

Identity

Trade Name
PREVENA™ CUSTOMIZABLE™ FDA UDI
Generic Name
Negative-pressure wound therapy system, electric, single-use FDA UDI
Device Name
Prevena Incision Management System- Customizable Dressing FDA UDI
Model / Reference
PRE2001US FDA UDI
Description
Prevena Incision Management System- Customizable Dressing FDA UDI

Identifiers

Primary DI / UDI-DI
00849554000056 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Negative-pressure wound therapy system, electric, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Negative-pressure wound therapy system, electric, single-use

Prevena™ Customizable™ by Kci Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system, electric, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kci Usa, Inc.

Sources (1)

  • FDA UDI a573a61a-1ee6-499e-af79-ac2604cb96f6 33 fields · synced May 31, 2026