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Pro Advantage

FDA UDI

Class I (US FDA UDI)

by National Distribution & Contracting, Inc.

Identity

Trade Name
Pro Advantage FDA UDI
Generic Name
Non-adhesive device retention bandage FDA UDI
Device Name
PA BANDAGE COHESIVE 1X5YD TAN 30/BX - (BX) FDA UDI
Model / Reference
P154010 FDA UDI
Description
PA BANDAGE COHESIVE 1X5YD TAN 30/BX - (BX) FDA UDI

Identifiers

Catalog Number
P154010 FDA UDI
Primary DI / UDI-DI
M220P1540103 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Non-adhesive device retention bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-adhesive device retention bandage

Pro Advantage by National Distribution & Contracting, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-adhesive device retention bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c8744e39-254d-4b51-a1cd-f559db8e4cbd 34 fields · synced Jun 8, 2026