← Back to catalogue

Tegaderm™

FDA UDI

Class U (US FDA UDI)

by 3m Company

Identity

Trade Name
Tegaderm™ FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI
Device Name
3M(TM) Tegaderm(TM) Alginate Ag Silver Dressing 90301 FDA UDI
Model / Reference
90301 FDA UDI
Description
3M(TM) Tegaderm(TM) Alginate Ag Silver Dressing 90301 FDA UDI

Identifiers

Catalog Number
90301 FDA UDI
Primary DI / UDI-DI
30707387583591 FDA UDI
510(k) Number
K090453 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

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: Exudate-absorbent dressing, hydrophilic-gel, antimicrobial

Tegaderm™ by 3m Company — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

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 Company

Sources (1)

  • FDA UDI f34df99e-1f53-4d6b-9ad6-a740a3d8a6ec 36 fields · synced May 30, 2026