ProCure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name: ProCure FDA UDI
Generic Name: Woven gauze pad, non-antimicrobial FDA UDI
Device Name: Gauze Sponges, 4"x 4" 8-ply Non-Sterile - 200ea/pk 20pk/cs FDA UDI
Model / Reference: PCGN448B FDA UDI
Description: Gauze Sponges, 4"x 4" 8-ply Non-Sterile - 200ea/pk 20pk/cs FDA UDI

Identifiers

Catalog Number: PCGN448B FDA UDI
Primary DI / UDI-DI: 10840330702383 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Woven gauze pad, non-antimicrobial 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 4 Inch FDA UDI
Length — 4 Inch FDA UDI

Category: Woven gauze pad, non-antimicrobial

ProCure by Twin Med, LLC — 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: Twin Med, LLC

Sources (1)

FDA UDI 365129c6-909f-4742-b63d-30b56c3bf767 36 fields · synced May 30, 2026