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Family Wellness

FDA UDI

Class I (US FDA UDI)

by Family Dollar Stores

Identity

Trade Name
Family Wellness FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
Small Gauze Pads, all one size, 2 IN x 2 IN (50 mm x 50 mm) FDA UDI
Model / Reference
032251058158 FDA UDI
Description
Small Gauze Pads, all one size, 2 IN x 2 IN (50 mm x 50 mm) FDA UDI

Identifiers

Catalog Number
0910867 FDA UDI
Primary DI / UDI-DI
00032251058158 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-woven gauze pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

Family Wellness by Family Dollar Stores — 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 b7fc2d1a-336a-4b1a-bf2d-5ee3f73c0de0 35 fields · synced May 30, 2026