Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

Peripheral vascular guidewire, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 70177. The device is manufactured by phenox GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is phenox UK Ltd.

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Peripheral vascular guidewire, manual

MHRA Device ID: 70177•Ref: 70177

Device Type

General Medical Device

Devices

Peripheral vascular guidewire, manual

Type

Class III

Date Registered

Apr 11, 2024

Last Updated

Mar 22, 2024

Manufacturer Information

Name

phenox GmbH

Address

Lise-Meitner-Allee 31

Bochum, Germany

Created Date

Mar 17, 2021

Authorized Representative

Name

phenox UK Ltd

Relationship Type

UK Responsible Person

Address

Phenox UK Ltd 23 Greenbox Westonhall Road Stoke Prior

Bromsgrove, England, United Kingdom

Postcode: B60 4AL

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Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

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