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ProStat

FDA UDI

Class I (US FDA UDI)

by Prostat First Aid, LLC

Identity

Trade Name
ProStat FDA UDI
Generic Name
First aid absorbent pad/bandage FDA UDI
Device Name
GAUZE ROLL 2" X 6 YD FDA UDI
Model / Reference
2279 FDA UDI
Description
GAUZE ROLL 2" X 6 YD FDA UDI

Identifiers

Primary DI / UDI-DI
00814889010629 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
First aid absorbent pad/bandage 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid absorbent pad/bandage

ProStat by Prostat First Aid, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid absorbent pad/bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8c879b25-f138-4294-8141-43f4fb55f598 33 fields · synced May 30, 2026