Fabco

FDA UDI

Class I (US FDA UDI)

by First Aid Bandage Co Inc

Identity

Trade Name: FABCO FDA UDI
Generic Name: Non-woven gauze pad FDA UDI
Model / Reference: 34771010 FDA UDI

Identifiers

Catalog Number: 34771010 FDA UDI
Primary DI / UDI-DI: 30634303020574 FDA UDI
FDA Product Code: FRL FDA UDI
GMDN Term: Non-woven gauze pad FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 1 Inch FDA UDI
Outer Diameter — 25.4 Millimeter FDA UDI

Category: Non-woven gauze pad

Fabco by First Aid Bandage Co Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: First Aid Bandage Co Inc

Sources (1)

FDA UDI 277b2d6f-32fe-4b00-87a1-8fc5bcd3e16f 35 fields · synced Jun 8, 2026