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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
Synthetic polymer semi-permeable film dressing, adhesive, non-sterile FDA UDI
Device Name
16004 3M Tegaderm Roll 10cm x 10m, 4 RLS/CS FDA UDI
Model / Reference
16004 FDA UDI
Description
16004 3M Tegaderm Roll 10cm x 10m, 4 RLS/CS FDA UDI

Identifiers

Catalog Number
16004 FDA UDI
Primary DI / UDI-DI
50707387565409 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, adhesive, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Synthetic polymer semi-permeable film dressing, adhesive, non-sterile

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

Similar devices

Also classified as Synthetic polymer semi-permeable film dressing, adhesive, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 1f1f5ba1-bccd-4cfd-ac6b-7a425f66317c 35 fields · synced Jun 8, 2026