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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 91384. The device is manufactured by Shenzhen Dongdixin Technology Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is Etheria Medical Ltd.

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General Medical Device
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Perineal orifice incontinence-control electrical stimulation system probe, reusable
MHRA Device ID: 91384โ€ขRef: 91384

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

Jul 9, 2024

Manufacturer Information

Address

Floor 1-2, No.3 Building, Fanshen Xusheng Industrial Estate Xilixiaobaimang 518108 Nanshan District

Shenzhen, China

Created Date

Jul 20, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

The Old brush Factory Unit 2D Whickham Industrial Estate, Swalwell

Newcastle Upon Tyne, United Kingdom

Postcode: NE16 3DA

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