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ARK™ Methotrexate II Calibrator

FDA UDI

Class U (US FDA UDI)

by Ark Diagnostics Inc

Identity

Trade Name
ARK™ Methotrexate II Calibrator FDA UDI
Generic Name
Methotrexate therapeutic drug monitoring IVD, calibrator FDA UDI
Device Name
ARK™ Methotrexate II Calibrator is intended for use in calibration of the ARK Methotrexate II Assay. FDA UDI
Model / Reference
5071-0002-00 FDA UDI
Description
ARK™ Methotrexate II Calibrator is intended for use in calibration of the ARK Methotrexate II Assay. FDA UDI

Identifiers

Catalog Number
5071-0002-00 FDA UDI
Primary DI / UDI-DI
00812101031186 FDA UDI
510(k) Number
K232017 FDA UDI
FDA Product Code
LAO FDA UDI
GMDN Term
Methotrexate therapeutic drug monitoring IVD, calibrator FDA UDI

Classification

Device Class
U 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

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: Methotrexate therapeutic drug monitoring IVD, calibrator

ARK™ Methotrexate II Calibrator by Ark Diagnostics Inc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Methotrexate therapeutic drug monitoring IVD, calibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ark Diagnostics Inc

Sources (1)

  • FDA UDI 3d1c40ce-59ae-4495-b62d-75de8b5bd60b 37 fields · synced May 30, 2026