Tissue embedding mould IVD, single-use - UK MHRA Medical Device Registration
Tissue embedding mould IVD, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135022. The device is manufactured by Sakura Finetek USA, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group 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.
Device Type
In Vitro Diagnostic Device
Devices
Tissue embedding mould IVD, single-use
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Address
1750 West 214th Street
Torrance, California , United States
Created Date
Feb 3, 2022
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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