← Back to catalogue

Liquid Ultra

FDA UDI

Class I (US FDA UDI)

by Crosstex International, Inc.

Identity

Trade Name
Liquid Ultra FDA UDI
Generic Name
Hydrogen peroxide device sterilant FDA UDI
Device Name
Dental Unit Waterline Treatment Solution FDA UDI
Model / Reference
DS503L FDA UDI
Description
Dental Unit Waterline Treatment Solution FDA UDI

Identifiers

Primary DI / UDI-DI
10732224000593 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Hydrogen peroxide device sterilant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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

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

No

FDA UDI

Category: Hydrogen peroxide device sterilant

Liquid Ultra by Crosstex International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydrogen peroxide device sterilant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e10b1d40-7c8b-49e4-9644-d8b92c12ece6 34 fields · synced Jun 8, 2026