Block-monitoring peripheral nerve electrical stimulation system - UK MHRA Medical Device Registration
Block-monitoring peripheral nerve electrical stimulation system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 206798. The device is manufactured by Senzime AB from Sweden, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class I
Status
Date Registered
Dec 12, 2024
Name
Senzime ABAddress
Company No: 556565-5734, , Verkstadsgatan 8,, Uppsala, Sweden
Uppsala, Sweden
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Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Dec 21, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Dec 21, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024
Block-monitoring peripheral nerve electrical stimulation system
Type: General Medical Device
Registered: Nov 26, 2024

