Fabco

FDA UDI

Class I (US FDA UDI)

by First Aid Bandage Co Inc

Identity

Trade Name: FABCO FDA UDI
Generic Name: Woven gauze pad, non-antimicrobial FDA UDI
Model / Reference: 34340810 FDA UDI

Identifiers

Catalog Number: 34340810 FDA UDI
Primary DI / UDI-DI: 30634303020338 FDA UDI
FDA Product Code: GDY FDA UDI
GMDN Term: Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4450 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: Width — 203.2 Millimeter FDA UDI
Length — 4 Inch FDA UDI
Length — 101.6 Millimeter FDA UDI
Width — 8 Inch FDA UDI

Category: Woven gauze pad, non-antimicrobial

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 9051a3fa-5ac1-4f2f-8721-8e40a834c5e6 35 fields · synced May 31, 2026