External defibrillation electrode, adult, single-use - UK MHRA Medical Device Registration

External defibrillation electrode, adult, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 198117. The device is manufactured by Progetti S.r.l from Italy, classified as General Medical Device. The authorized representative in the UK is Obelis UK 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.

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External defibrillation electrode, adult, single-use

MHRA Device ID: 198117•Ref: 198117

Device Type

General Medical Device

Devices

External defibrillation electrode, adult, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 20, 2024

Manufacturer Information

Name

Progetti S.r.l

Address

Strada del Rondello 5

Trofarello (Turin), Italy

Created Date

Jan 2, 2024

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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External defibrillation electrode, adult, single-use - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Created Date

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Address

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