General specimen collection kit IVD, clinical - UK MHRA Medical Device Registration

General specimen collection kit IVD, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 132484. The device is manufactured by JINAN BABIO BIOTECHNOLOGY CO., LTD. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is PureUKCA 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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General specimen collection kit IVD, clinical

MHRA Device ID: 132484•Ref: 132484

Device Type

In Vitro Diagnostic Device

Devices

General specimen collection kit IVD, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 13, 2024

Manufacturer Information

Name

JINAN BABIO BIOTECHNOLOGY CO., LTD.

Address

303, Building 5 of SME Industrialization Base of Biomedical Park, 1777 Dazheng Road, High-tech Zone, Jinan City, 250101, Shandong Province, China

Jinan, Shandong, China

Created Date

Jun 1, 2021

Authorized Representative

Name

PureUKCA Ltd

Relationship Type

UK Responsible Person

Address

59 St. Martin's Lane

London, Middlesex, England, United Kingdom

Postcode: WC2N 4JS

DJ Fang

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Other Products from JINAN BABIO BIOTECHNOLOGY CO., LTD. (2)

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Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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General specimen collection kit IVD, clinical - UK MHRA Medical Device Registration

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