← Back to catalogue

Tegaderm™

FDA UDI

Class U (US FDA UDI)

by 3m Company

Identity

Trade Name
Tegaderm™ FDA UDI
Generic Name
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
3M™ Tegaderm™ CHG Dressing 25/Carton 4 Cartons/Case 1657 FDA UDI
Model / Reference
1657 FDA UDI
Description
3M™ Tegaderm™ CHG Dressing 25/Carton 4 Cartons/Case 1657 FDA UDI

Identifiers

Catalog Number
1657 FDA UDI
Primary DI / UDI-DI
30707387578313 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive 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

Category: Antimicrobial synthetic polymer semi-permeable film dressing, adhesive

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

Similar devices

Also classified as Antimicrobial synthetic polymer semi-permeable film dressing, adhesive.

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 9d01afd3-7bcd-48f4-9025-142b9b1e0533 35 fields · synced May 29, 2026