Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91264. The device is manufactured by EPflex Feinwerktechnik GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL UK LIMITED.

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 91264•Ref: 91264

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jun 6, 2024

Manufacturer Information

Name

EPflex Feinwerktechnik GmbH

Address

Im Schwöllbogen 24

Dettingen an der Erms , Germany

Created Date

Jul 30, 2021

Authorized Representative

Name

MEDAGENT INTERNATIONAL UK LIMITED

Relationship Type

UK Responsible Person

Address

2 St Andrews Place

Lewes, East Sussex, England, United Kingdom

Postcode: BN7 1UP

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Other Products from EPflex Feinwerktechnik GmbH (3)

Other Products from Same Authorized Representative (10)

Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Cardiac/peripheral vascular guidewire, single-use

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