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Solujet

FDA UDI

Class I (US FDA UDI)

by Alconox, LLC

Identity

Trade Name
Solujet FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Cleaner for ultrasonic cleaning of medical devices FDA UDI
Model / Reference
30 Gallon FDA UDI
Description
Cleaner for ultrasonic cleaning of medical devices FDA UDI

Identifiers

Catalog Number
2130 FDA UDI
Primary DI / UDI-DI
00660483213016 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device cleaning agent

Solujet by Alconox, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alconox, LLC

Sources (1)

  • FDA UDI d9620c89-fe3d-457b-b14b-c5f40257f1ce 35 fields · synced Jun 9, 2026