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Craniofacial analgesia electrical stimulator - UK MHRA Medical Device Registration

Craniofacial analgesia electrical stimulator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204964. The device is manufactured by CEFALY Technology from Belgium, classified as General Medical Device. The authorized representative in the UK is International Associates 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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Craniofacial analgesia electrical stimulator
MHRA Device ID: 204964โ€ขRef: 204964

Device Type

General Medical Device

Devices

Craniofacial analgesia electrical stimulator

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 14, 2024

Manufacturer Information

Address

Boulevard Patience et Beaujonc 3, bte 28

Liรจge, Belgium

Created Date

Nov 12, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

38 Queen Street

Glasgow, Scotland, United Kingdom

Postcode: G1 3DX

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