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Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, radioimmunoassay - UK MHRA Medical Device Registration

Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, radioimmunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 162248. The device is manufactured by Immunotech s.r.o from Czechia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Beckman Coulter UK Ltd.

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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Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, radioimmunoassay
MHRA Device ID: 162248โ€ขRef: 162248

Device Type

In Vitro Diagnostic Device

Devices

Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, radioimmunoassay

Type

Class C

Date Registered

Feb 23, 2024

Last Updated

Feb 2, 2024

Manufacturer Information

Address

Radiova 1122/1 102 00 Prague 10

Prague, Czechia

Created Date

Aug 3, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Oakley Court Kingsmead Busines sPark London Rd

High Wycombe, Bucks, United Kingdom

Postcode: HP11 1JU

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