Pure Global

ARK Diagnostics, Inc. - Medical Device Manufacturer in United Kingdom

ARK Diagnostics, Inc. from United States is a medical device manufacturer with 20 registered products in the UK MHRA database through Pure Global AI's free platform. The company produces 20 unique generic names across 1 device type.

This page provides comprehensive manufacturer intelligence including complete product portfolio and device type distribution. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify manufacturers, analyze portfolios, and discover partnership opportunities efficiently.

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20 Products
1 Types
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ARK Diagnostics, Inc.
United States

48089 Fremont Blvd

Fremont, United States

20
Total Products
20
Generic Names
1
Device Types
20
Generic Names
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Recent Registrations (20 most recent)
Most recently registered products with MHRA

2-ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

140389

Registration Date:

Nov 26, 2024

Ethyl glucuronide (EtG) IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

140391

Registration Date:

Nov 26, 2024

Fentanyl IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

111700

Registration Date:

Nov 26, 2024

Ketamine/ketamine metabolite IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

111711

Registration Date:

Nov 26, 2024

Methotrexate therapeutic drug monitoring IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

111693

Registration Date:

Nov 26, 2024

Neurontin (gabapentin) IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

111705

Registration Date:

Nov 26, 2024

Pethidine IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

140403

Registration Date:

Nov 26, 2024

Pethidine IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

140395

Registration Date:

Nov 26, 2024

Pethidine IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

140394

Registration Date:

Nov 26, 2024

Pregabalin IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

111703

Registration Date:

Nov 26, 2024

Synthetic cannabinoid/synthetic cannabinoid metabolite IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

140399

Registration Date:

Nov 26, 2024

Tramadol IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

111709

Registration Date:

Nov 26, 2024

Tramadol IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

111708

Registration Date:

Nov 26, 2024

Voriconazole therapeutic drug monitoring IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

111704

Registration Date:

Nov 26, 2024

Voriconazole therapeutic drug monitoring IVD, reagent

Type:

In Vitro Diagnostic Device

Device ID:

111713

Registration Date:

Nov 26, 2024

2-ethylidine-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

140390

Registration Date:

Nov 26, 2024

Ethyl glucuronide (EtG) IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

140392

Registration Date:

Nov 26, 2024

Fentanyl IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

111715

Registration Date:

Nov 26, 2024

Gabapentin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

111707

Registration Date:

Nov 26, 2024

Pregabalin IVD, calibrator

Type:

In Vitro Diagnostic Device

Device ID:

111702

Registration Date:

Nov 26, 2024