Intravenous pressure infusor, manual, single-use - UK MHRA Medical Device Registration
Intravenous pressure infusor, manual, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195241. The device is manufactured by Shenzhen Caremed Medical Technology 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.
Device Type
General Medical Device
Devices
Intravenous pressure infusor, manual, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jun 20, 2024
Address
3/F, Building C, Xiazao digital industrial park, No.8 Huali road, Gaofeng community, Dalang office, Longhua district
Shenzhen, China
Created Date
Jun 13, 2024
Name
MedPath LimitedRelationship Type
Address
27 Old Gloucester Street
London, England, United Kingdom
Postcode: WC1N 3AX
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