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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-woven gauze pad FDA UDI
Device Name
PRO ADVANTAGE PAD NON ADHERENT ST 3X4 100/BX 12BX/CS FDA UDI
Model / Reference
P150160 FDA UDI
Description
PRO ADVANTAGE PAD NON ADHERENT ST 3X4 100/BX 12BX/CS FDA UDI

Identifiers

Catalog Number
P150160 FDA UDI
Primary DI / UDI-DI
M220P1501603 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Non-woven gauze pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-woven gauze pad

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-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c693d83-9664-4bf7-a0c0-4a5ed0d1d52f 35 fields · synced May 30, 2026