← Back to catalogue

3M™ Tegaderm™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
3M™ Tegaderm™ FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Device Name
3M™ Tegaderm™ High Performance Foam Non-Adhesive Dressing, 90604, Fenestrated, 3.5 in x 3.5 in, 10/CAR, 4 CAR/CS, 40/CS FDA UDI
Model / Reference
90604 FDA UDI
Description
3M™ Tegaderm™ High Performance Foam Non-Adhesive Dressing, 90604, Fenestrated, 3.5 in x 3.5 in, 10/CAR, 4 CAR/CS, 40/CS FDA UDI

Identifiers

Catalog Number
90604 FDA UDI
Primary DI / UDI-DI
00707387815523 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Exudate-absorbent dressing, non-gel, non-antimicrobial

3M™ Tegaderm™ by 3M Deutschland GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, non-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI f234f231-fd17-4263-8772-12618df9bd4d 35 fields · synced Jun 1, 2026