Peripheral angioplasty balloon catheter, basic - UK MHRA Medical Device Registration

Peripheral angioplasty balloon catheter, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92017. The device is manufactured by AV Medical Technologies Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.

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Peripheral angioplasty balloon catheter, basic

MHRA Device ID: 92017•Ref: 92017

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

May 14, 2024

Manufacturer Information

Name

AV Medical Technologies Ltd.

Address

21B Habarzel St.

Tel Aviv , Israel

Created Date

Aug 3, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Peripheral angioplasty balloon catheter, basic - UK MHRA Medical Device Registration

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