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 111542. The device is manufactured by InMode Ltd from Israel, classified as General Medical Device. The authorized representative in the UK is UKCApartner4U 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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Perineal orifice incontinence-control electrical stimulation system probe, reusable

MHRA Device ID: 111542•Ref: 111542

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

Nov 19, 2024

Manufacturer Information

Name

InMode Ltd

Address

1 Carmel Street Tavor Building Shaar Yokneam

Yokneam, Israel

Created Date

Nov 8, 2021

Authorized Representative

Name

UKCApartner4U Limited

Relationship Type

UK Responsible Person

Address

7 CAMPION WAY

BINGHAM, NOTTINGHAM, England, United Kingdom

Postcode: NG13 8 TR

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

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Address

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