Pure Global

UTAK Laboratories Inc. - Medical Device Manufacturer in United Kingdom

UTAK Laboratories 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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UTAK Laboratories Inc.
United States

25020 Avenue Tibbitts Valencia

CA, 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

Ketamine/ketamine metabolite IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88252

Registration Date:

Nov 26, 2024

Methylphenidate metabolite IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88261

Registration Date:

Nov 26, 2024

Multiple antifungal therapeutic drug monitoring IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88260

Registration Date:

Nov 26, 2024

Multiple form 25-hydroxy Vitamin D IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88229

Registration Date:

Nov 26, 2024

Amphetamine/methamphetamine group IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88233

Registration Date:

Nov 26, 2024

Cocaine/cocaine metabolite IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88237

Registration Date:

Nov 26, 2024

Multiple therapeutic drugs/drugs of abuse IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88221

Registration Date:

Nov 26, 2024

Multiple vitamin IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88228

Registration Date:

Nov 26, 2024

Nortriptyline IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88223

Registration Date:

Nov 26, 2024

Pethidine IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88255

Registration Date:

Nov 26, 2024

Phenobarbital IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88247

Registration Date:

Nov 26, 2024

Multiple antidepressant therapeutic drug monitoring IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88254

Registration Date:

Nov 26, 2024

Benzodiazepine group IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88235

Registration Date:

Nov 26, 2024

Buprenorphine IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88224

Registration Date:

Nov 26, 2024

Lead IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88226

Registration Date:

Nov 26, 2024

Methotrexate therapeutic drug monitoring IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88222

Registration Date:

Nov 26, 2024

Methylmalonic acid (MMA) IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88227

Registration Date:

Nov 26, 2024

Morphine/morphine metabolite IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88243

Registration Date:

Nov 26, 2024

Multiple heavy metal IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88230

Registration Date:

Nov 26, 2024

Carisoprodol IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

88256

Registration Date:

Nov 26, 2024