Vascular dilator, single-use - UK MHRA Medical Device Registration

Vascular dilator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210382. The device is manufactured by Cordis US Corp. from United States, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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MHRA Registered

General Medical Device

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Vascular dilator, single-use

MHRA Device ID: 210382

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Feb 11, 2025

Manufacturer Information

Name

Cordis US Corp.

Address

14201 North West 60th Avenue

Miami Lakes, Florida, United States

DJ Fang

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Vascular dilator, single-use - UK MHRA Medical Device Registration

Device Type

Type

Status

Date Registered

Name

Address

DJ Fang

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