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3m™ V.a.c.®

FDA UDI

Class II (US FDA UDI)

by Kci Usa, Inc.

Identity

Trade Name
3M™ V.A.C.® FDA UDI
Generic Name
Negative-pressure wound therapy system foam dressing, non-antimicrobial FDA UDI
Device Name
3M™ V.A.C.® Peel and Place Dressing Kit, EZ5LRG, Large, 5/CS FDA UDI
Model / Reference
EZ5LRGV001 / EZ5LRGV002 FDA UDI
Description
3M™ V.A.C.® Peel and Place Dressing Kit, EZ5LRG, Large, 5/CS FDA UDI

Identifiers

Catalog Number
EZ5LRG FDA UDI
Primary DI / UDI-DI
10849554013886 FDA UDI
510(k) Number
K222859 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Negative-pressure wound therapy system foam dressing, non-antimicrobial 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

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

3m™ V.a.c.® 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 foam dressing, non-antimicrobial.

Cleared under the same submission

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 bc276a03-570c-4f37-9cab-cf1047ac1779 36 fields · synced May 30, 2026