Vascular guide-catheter, single-use - UK MHRA Medical Device Registration

Vascular guide-catheter, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 200157. The device is manufactured by Reflow Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Medes Ltd..

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Vascular guide-catheter, single-use

MHRA Device ID: 200157•Ref: 200157

Device Type

General Medical Device

Devices

Vascular guide-catheter, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 7, 2024

Manufacturer Information

Name

Reflow Medical, Inc.

Address

208 Avenida Fabricante, Suite 100

San Clemente,, California, United States

Created Date

Sep 4, 2024

Authorized Representative

Name

Medes Ltd.

Relationship Type

UK Responsible Person

Address

5 Beaumont Gate, Shenley Hil

Radlett, Herts, England, United Kingdom

Postcode: WD77AR

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Other Products from Reflow Medical, Inc. (1)

Peripheral artery stent, bare-metal

Type: General Medical Device

Registered: Nov 26, 2024

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Vascular guide-catheter, single-use - UK MHRA Medical Device Registration

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