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 98089. The device is manufactured by Laborie Medical Technologies. Corp. from United States, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Perineal orifice incontinence-control electrical stimulation system probe, reusable

MHRA Device ID: 98089•Ref: 98089

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

Oct 31, 2024

Manufacturer Information

Name

Laborie Medical Technologies. Corp.

Address

180 International Drive

New Hampshire, Portsmouth, United States

Created Date

Aug 24, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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

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Last Updated

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Created Date

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Address

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