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ASI Rubella Test

FDA UDI

Class II (US FDA UDI)

by Arlington Scientific, Inc.

Identity

Trade Name
ASI Rubella Test FDA UDI
Generic Name
Rubella virus total antibody IVD, kit, rapid agglutination, clinical FDA UDI
Device Name
Detection of Rubella Virus Antibodies, Export FDA UDI
Model / Reference
NC-600100E FDA UDI
Description
Detection of Rubella Virus Antibodies, Export FDA UDI

Identifiers

Catalog Number
NC-600100E FDA UDI
Primary DI / UDI-DI
00816057020430 FDA UDI
510(k) Number
K031490 FDA UDI
FDA Product Code
LQN FDA UDI
GMDN Term
Rubella virus total antibody IVD, kit, rapid agglutination, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3510 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

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: Rubella virus total antibody IVD, kit, rapid agglutination, clinical

ASI Rubella Test by Arlington Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubella virus total antibody IVD, kit, rapid agglutination, clinical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 07fcc37f-5051-4f36-933a-9873e40936c1 38 fields · synced Jul 18, 2026