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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
Cavity-wound management dressing, non-antimicrobial FDA UDI
Device Name
3M™ TEGADERM™ HYDROGEL WOULD FILLER 91110 FDA UDI
Model / Reference
91110 FDA UDI
Description
3M™ TEGADERM™ HYDROGEL WOULD FILLER 91110 FDA UDI

Identifiers

Catalog Number
91110 FDA UDI
Primary DI / UDI-DI
30707387564095 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Cavity-wound management dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 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

No

FDA UDI

Category: Cavity-wound management dressing, non-antimicrobial

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

Similar devices

Also classified as Cavity-wound management dressing, 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 e7a825d3-b738-41e3-927e-348c1e590c0f 35 fields · synced May 30, 2026