Prabadin

FDA UDI

Class I (US FDA UDI)

by Prabadin Corp

Identity

Trade Name: PRABADIN FDA UDI
Generic Name: Woven gauze pad, non-antimicrobial FDA UDI
Device Name: Gauze sponge, 4x4x16ply, Xray detectable, sterile FDA UDI
Model / Reference: PR71AC-16P FDA UDI
Description: Gauze sponge, 4x4x16ply, Xray detectable, sterile FDA UDI

Identifiers

Primary DI / UDI-DI: 00850051158232 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

Category: Woven gauze pad, non-antimicrobial

Prabadin by Prabadin Corp — 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: Prabadin Corp

Sources (1)

FDA UDI 7b998578-f728-4c5f-9614-2b2c46535323 34 fields · synced Jun 8, 2026