Dental suction system cannula, single-use - UK MHRA Medical Device Registration

Dental suction system cannula, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160459. The device is manufactured by Crosstex International Inc. from United States, classified as General Medical Device. The authorized representative in the UK is STERIS Solutions 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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Dental suction system cannula, single-use

MHRA Device ID: 160459•Ref: 160459

Device Type

General Medical Device

Devices

Dental suction system cannula, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 25, 2024

Manufacturer Information

Name

Crosstex International Inc.

Address

6789 W. Henrietta Road Rush

New York, United States

Created Date

Nov 11, 2022

Authorized Representative

Name

STERIS Solutions Limited

Relationship Type

UK Responsible Person

Address

Chancery House, Rayns Way Watermead Business Park Syston

Leicester, Leicestershire, England, United Kingdom

Postcode: LE7 1PF

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Dental suction system cannula, single-use - UK MHRA Medical Device Registration

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