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General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 136749. The device is manufactured by Mawi DNA Technologies LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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In Vitro Diagnostic Device
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General specimen container IVD, additive/medium
MHRA Device ID: 136749โ€ขRef: 136749

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 19, 2024

Manufacturer Information

Address

1252 Quarry Lane Suite A

Pleasanton, California, United States

Created Date

Feb 16, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

7 CAMPION WAY

BINGHAM, NOTTINGHAM, England, United Kingdom

Postcode: NG13 8 TR

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