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General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 149651. The device is manufactured by Liofilchem S.r.l. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics 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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In Vitro Diagnostic Device
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General specimen container IVD, additive/medium
MHRA Device ID: 149651Ref: 149651

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Apr 5, 2024

Manufacturer Information

Address

Via Scozia Zona industriale ROSETO DEGLI ABRUZZI

TE, Abruzzo, Italy

Created Date

Apr 29, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

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