← Back to catalogue

ASI Evolution RPR Titration Diluent

FDA UDI

Class II (US FDA UDI)

by Arlington Scientific, Inc.

Identity

Trade Name
ASI Evolution RPR Titration Diluent FDA UDI
Generic Name
Treponema pallidum reagin antibody IVD, kit, agglutination FDA UDI
Device Name
RPR Sample Diluent used on the ASI Evolution Analyzer for performing sample titrations. 25 ml FDA UDI
Model / Reference
NC-5300-905A FDA UDI
Description
RPR Sample Diluent used on the ASI Evolution Analyzer for performing sample titrations. 25 ml FDA UDI

Identifiers

Catalog Number
NC-5300-905A FDA UDI
Primary DI / UDI-DI
00816057021710 FDA UDI
FDA Product Code
GMQ FDA UDI
GMDN Term
Treponema pallidum reagin antibody IVD, kit, agglutination FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3820 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

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

No

FDA UDI

Category: Treponema pallidum reagin antibody IVD, kit, agglutination

ASI Evolution RPR Titration Diluent by Arlington Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Treponema pallidum reagin antibody IVD, kit, agglutination.

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 eefbe949-67ba-4d7c-a480-70607ad87512 35 fields · synced Jul 18, 2026