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 73443. The device is manufactured by Datascope Corp. from United States, classified as General Medical Device. The authorized representative in the UK is Getinge Limited.

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 73443•Ref: 73443

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 23, 2024

Manufacturer Information

Name

Datascope Corp.

Address

1300 MacArthur Blvd

Mahwah,, United States

Created Date

Apr 15, 2021

Authorized Representative

Name

Getinge Limited

Relationship Type

UK Responsible Person

Address

Unit 3 St Modwen Park Andressey Way Chaddesden

Derby, England, United Kingdom

Postcode: DE21 6YH

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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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