Needle guide, reusable - UK MHRA Medical Device Registration
Needle guide, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169390. The device is manufactured by MEDICAP Srl from Italy, classified as General Medical Device. The authorized representative in the UK is MDQ Services 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
General Medical Device
Devices
Needle guide, reusable
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Sep 3, 2024
Name
MDQ Services LtdRelationship Type
Address
Flat 81, Seacon Tower, 5 Hutchingโs Street
London, England, England, United Kingdom
Postcode: E14 8JX
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