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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 103459. The device is manufactured by APT Medical Inc. from China, classified as General Medical Device. The authorized representative in the UK is Jump Start Consulting Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Cardiac/peripheral vascular guidewire, single-use
MHRA Device ID: 103459โ€ขRef: 103459

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Aug 1, 2024

Manufacturer Information

Address

Room 601, Building B, Tongfang Information Port No.11 Langshan Road, Nanshan District

Shenzhen, China

Created Date

Sep 9, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit 24 Cranfield Innovation Centre University Way

Cranfield, Bedfordshire, England, United Kingdom

Postcode: MK43 0BT

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