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 96411. The device is manufactured by Spectranetics Corporation - Brandin Court from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

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Peripheral angioplasty balloon catheter, basic

MHRA Device ID: 96411•Ref: 96411

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Sep 29, 2024

Last Updated

Feb 1, 2024

Manufacturer Information

Name

Spectranetics Corporation - Brandin Court

Address

5055 Brandin Court

Fremont, United States

Created Date

Apr 26, 2021

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

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Other Products from Spectranetics Corporation - Brandin Court (1)

Coronary angioplasty balloon catheter, cutting/scoring

Type: General Medical Device

Registered: Sep 29, 2024

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

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