Identity
- Trade Name
- ARK™ Methotrexate II Assay FDA UDI
- Generic Name
- Methotrexate therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- The ARK™ Methotrexate II Assay is a homogeneous enzyme immunoassay intended for the quantitative determination of methotrexate in human serum or plasma on automated clinical chemistry analyzers. FDA UDI
- Model / Reference
- 5071-0001-01 FDA UDI
- Description
- The ARK™ Methotrexate II Assay is a homogeneous enzyme immunoassay intended for the quantitative determination of methotrexate in human serum or plasma on automated clinical chemistry analyzers. FDA UDI
Identifiers
- Catalog Number
- 5071-0001-01 FDA UDI
- Primary DI / UDI-DI
- 00812101031179 FDA UDI
- 510(k) Number
- K232017 FDA UDI
- FDA Product Code
- LAO FDA UDI
- GMDN Term
- Methotrexate therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) 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, kit, enzyme immunoassay (EIA)
ARK™ Methotrexate II Assay 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, kit, enzyme immunoassay (EIA).
- ONLINE TDM Methotrexate — Roche Diagnostics Corp. · U
- ONLINE TDM Methotrexate — Roche Diagnostics Corp. · U
- Syva® Emit® Methotrexate Assay — Siemens Healthcare Diagnostics · U
- ARK™ Methotrexate Assay — ARK DIAGNOSTICS INC · U
- ARK™ Methotrexate II Assay — ARK DIAGNOSTICS INC · U
- ARK™ Methotrexate Assay (c-pack) — ARK DIAGNOSTICS INC · U
- ARK™ Methotrexate Assay — ARK DIAGNOSTICS INC · U
- ARK™ Methotrexate Assay — ARK DIAGNOSTICS INC · U
Cleared under the same submission
K232017 also covers:
- ARK™ Methotrexate II Assay — ARK DIAGNOSTICS INC
- ARK™ Methotrexate II Calibrator — ARK DIAGNOSTICS INC
- ARK™ Methotrexate II Control — ARK DIAGNOSTICS INC
- ARK™ Methotrexate II Control — ARK DIAGNOSTICS INC
- ARK™ Methotrexate II Control — ARK DIAGNOSTICS INC
- ARK™ Methotrexate II Dilution Buffer — ARK DIAGNOSTICS INC
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ark Diagnostics Inc
Sources (1)
- FDA UDI 3a56bdee-eabf-4227-a7d6-a2cb1926cf96 37 fields · synced May 30, 2026