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 133617. The device is manufactured by Everyway Medical Instruments Co., Ltd. from Taiwan, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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Perineal orifice incontinence-control electrical stimulation system probe, reusable

MHRA Device ID: 133617•Ref: 133617

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 10, 2023

Manufacturer Information

Name

Everyway Medical Instruments Co., Ltd.

Address

3Fl. & 8Fl., No.5, Ln. 155, Sec. 3, Beishen Rd. Shenkeng Dist.

New Taipei City, Taiwan

Created Date

Jan 24, 2022

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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

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