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AlphaCleanse

FDA UDI

Class II (US FDA UDI)

by Bionix, LLC

Identity

Trade Name
AlphaCleanse FDA UDI
Generic Name
Wound irrigation kit FDA UDI
Device Name
Sample, AlphaCleanse Antimicrobial Wound Care System FDA UDI
Model / Reference
25750 FDA UDI
Description
Sample, AlphaCleanse Antimicrobial Wound Care System FDA UDI

Identifiers

Catalog Number
25750 FDA UDI
Primary DI / UDI-DI
00714646000828 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Wound irrigation kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Total Volume — 8 Fluid Ounce FDA UDI

AlphaCleanse by Bionix, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bionix, LLC

Sources (1)

  • FDA UDI 419ffd29-9a99-44f2-8e49-85b8b8a0db79 38 fields · synced May 30, 2026