General specimen collection kit - UK MHRA Medical Device Registration

General specimen collection kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 162651. The device is manufactured by Finess Healthcare Group Co.,Ltd from China, classified as General Medical Device. The authorized representative in the UK is MedPath 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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General specimen collection kit

MHRA Device ID: 162651•Ref: 162651

Device Type

General Medical Device

Devices

General specimen collection kit

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 4, 2023

Manufacturer Information

Name

Finess Healthcare Group Co.,Ltd

Address

No.1503 A1 Block, No.203 Lantian Road

Ningbo, China

Created Date

Jan 17, 2022

Authorized Representative

Name

MedPath Limited

Relationship Type

UK Responsible Person

Address

27 Old Gloucester Street

London, England, United Kingdom

Postcode: WC1N 3AX

DJ Fang

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Other Products from Finess Healthcare Group Co.,Ltd (10)

Other Products from Same Authorized Representative (10)

General specimen collection kit - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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