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Citrajet

FDA UDI

Class I (US FDA UDI)

by Alconox, LLC

Identity

Trade Name
Citrajet FDA UDI
Generic Name
Instrument rinsing agent FDA UDI
Device Name
Cleaner for ultrasonic cleaning of medical devices FDA UDI
Model / Reference
1 Gallon FDA UDI
Description
Cleaner for ultrasonic cleaning of medical devices FDA UDI

Identifiers

Catalog Number
2001-1 FDA UDI
Primary DI / UDI-DI
00660483200115 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Instrument rinsing 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: Instrument rinsing agent

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

Similar devices

Also classified as Instrument rinsing 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 cbb32852-1818-455d-87fb-24e01c20aef6 35 fields · synced Jun 9, 2026