Perineal orifice incontinence-control electrical stimulation system probe, reusable - UK MHRA Medical Device Registration

Perineal orifice incontinence-control electrical stimulation system probe, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 111132. The device is manufactured by BEACMED S.r.l. 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.

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Perineal orifice incontinence-control electrical stimulation system probe, reusable

MHRA Device ID: 111132•Ref: 111132

Device Type

General Medical Device

Devices

Perineal orifice incontinence-control electrical stimulation system probe, reusable

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 3, 2024

Manufacturer Information

Name

BEACMED S.r.l.

Address

Via Monte Bianco 12

Portalbera, Pavia, Italy

Created Date

Sep 22, 2021

Authorized Representative

Name

MDQ Services Ltd

Relationship Type

UK Responsible Person

Address

Flat 81, Seacon Tower, 5 Hutching’s Street

London, England, England, United Kingdom

Postcode: E14 8JX

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Perineal orifice incontinence-control electrical stimulation system probe, reusable - UK MHRA Medical Device Registration

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