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3M™ Tegaderm™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
3M™ Tegaderm™ FDA UDI
Generic Name
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
3M™ Tegaderm™ I.V. Transparent Film Dressing with Adhesive-Free Window, 1668, 4-3/4 in x 4-3/4 in, 25/ct 4ct/Case FDA UDI
Model / Reference
1668 FDA UDI
Description
3M™ Tegaderm™ I.V. Transparent Film Dressing with Adhesive-Free Window, 1668, 4-3/4 in x 4-3/4 in, 25/ct 4ct/Case FDA UDI

Identifiers

Catalog Number
1668 FDA UDI
Primary DI / UDI-DI
30707387807666 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 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: Synthetic polymer semi-permeable film dressing, adhesive

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

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI e1f76f88-4604-48a3-9dec-fc263161a1ea 35 fields · synced May 31, 2026