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General specimen container IVD, no additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, no additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 167264. The device is manufactured by Siemens Healthcare Diagnostics Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Siemens Healthcare Diagnostics 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, no additive/medium
MHRA Device ID: 167264โ€ขRef: 167264

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, no additive/medium

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Nov 3, 2023

Manufacturer Information

Address

62 Flanders-Bartley Road

Flanders, NJ, United States

Created Date

Oct 19, 2017

Authorized Representative

Relationship Type

UK Responsible Person

Address

Park View Watchmoor Park

Surrey, Camberley, England, United Kingdom

Postcode: GU15 3YL

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