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3M™ Tegaderm™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Tegaderm™ FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Device Name
3M™ Tegaderm™ Silicone Foam Border Dressing 6x6IN 15x15CM 10EA/CAR 4CAR/CS 90642 FDA UDI
Model / Reference
90642 FDA UDI
Description
3M™ Tegaderm™ Silicone Foam Border Dressing 6x6IN 15x15CM 10EA/CAR 4CAR/CS 90642 FDA UDI

Identifiers

Catalog Number
90642 FDA UDI
Primary DI / UDI-DI
00707387776763 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

Yes

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

No

FDA UDI

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

3M™ Tegaderm™ by 3m Company — 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

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI f42d0486-873a-4dc4-a1c2-ce43d70def03 35 fields · synced Jun 1, 2026