← Back to catalogue

3M™ Nexcare™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Nexcare™ FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
Nexcare™ Advanced Healing Waterproof Hydrocolloid Pads, AHD-06, 6 ct. 3.93" x 2.96" FDA UDI
Model / Reference
AHD-06 FDA UDI
Description
Nexcare™ Advanced Healing Waterproof Hydrocolloid Pads, AHD-06, 6 ct. 3.93" x 2.96" FDA UDI

Identifiers

Catalog Number
AHD-06 FDA UDI
Primary DI / UDI-DI
30051131215680 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Adhesive bandage 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

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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Adhesive bandage

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

Similar devices

Also classified as Adhesive bandage.

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 f4ed0010-a3d8-4724-aab6-259b6a8929f0 35 fields · synced Jun 8, 2026