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Prabadin

FDA UDI

Class I (US FDA UDI)

by Prabadin Corp

Identity

Trade Name
PRABADIN FDA UDI
Generic Name
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI
Device Name
Gauze sponge, 4x4x12ply, non sterile FDA UDI
Model / Reference
PRGS4412PNS FDA UDI
Description
Gauze sponge, 4x4x12ply, non sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00850051158249 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, 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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wound-nonadherent dressing, permeable, non-antimicrobial

Prabadin by Prabadin Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, permeable, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Prabadin Corp

Sources (1)

  • FDA UDI 48e3ff7e-d594-46e7-a4e8-1791da098df4 34 fields · synced May 30, 2026