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3M™ Micropore™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Micropore™ FDA UDI
Generic Name
Hypoallergenic skin adhesive tape FDA UDI
Device Name
3M™ Micropore™ Paper Tape Plus 2 IN X 10 YD 6 Rolls/Carton 10 Cartons/Case 1532-2 FDA UDI
Model / Reference
1532-2 FDA UDI
Description
3M™ Micropore™ Paper Tape Plus 2 IN X 10 YD 6 Rolls/Carton 10 Cartons/Case 1532-2 FDA UDI

Identifiers

Catalog Number
1532-2 FDA UDI
Primary DI / UDI-DI
30707387763153 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Hypoallergenic skin adhesive tape 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: Hypoallergenic skin adhesive tape

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

Similar devices

Also classified as Hypoallergenic skin adhesive tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 26e95735-3e8a-448c-86ae-cdc93434eef1 35 fields · synced Jun 6, 2026