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Tissue cryostorage straw - UK MHRA Medical Device Registration

Tissue cryostorage straw is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 110713. The device is manufactured by REPROLIFE Inc. from Japan, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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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Tissue cryostorage straw
MHRA Device ID: 110713•Ref: 110713

Device Type

General Medical Device

Devices

Tissue cryostorage straw

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Aug 17, 2024

Manufacturer Information

Address

2-5-3 9F, Shinjuku, Shinjuku-ku

Tokyo, Japan

Created Date

Nov 3, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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