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3M™ Cavilon™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Cavilon™ FDA UDI
Generic Name
Synthetic-polymer liquid barrier dressing, sterile FDA UDI
Device Name
3M™ Cavilon™ No Sting Barrier Film Wipes, 0.75 ML, Carton of 100 Wipes, 3342K FDA UDI
Model / Reference
3342K FDA UDI
Description
3M™ Cavilon™ No Sting Barrier Film Wipes, 0.75 ML, Carton of 100 Wipes, 3342K FDA UDI

Identifiers

Catalog Number
3342K FDA UDI
Primary DI / UDI-DI
30707387787098 FDA UDI
510(k) Number
K955103 FDA UDI
FDA Product Code
KMF FDA UDI
GMDN Term
Synthetic-polymer liquid barrier dressing, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synthetic-polymer liquid barrier dressing, sterile

3M™ Cavilon™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic-polymer liquid barrier dressing, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 76c0fb7f-048b-4ce6-987c-1845ffd47b40 36 fields · synced Jun 8, 2026