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Advance Dental Products

FDA UDI

Class I (US FDA UDI)

by The Atlanta Dental Supply Company

Identity

Trade Name
Advance Dental Products FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
Sponges Non Woven 4 x 4 4ply FDA UDI
Model / Reference
7442000 FDA UDI
Description
Sponges Non Woven 4 x 4 4ply FDA UDI

Identifiers

Primary DI / UDI-DI
10371347000006 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

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-woven gauze pad

Advance Dental Products by The Atlanta Dental Supply Company — 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 a7933fae-76c4-4d86-ab48-187c38d5bb4b 33 fields · synced May 30, 2026