Phacoemulsification system handpiece - UK MHRA Medical Device Registration

Phacoemulsification system handpiece is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92150. The device is manufactured by Bausch & Lomb Incorporated from United States, classified as General Medical Device. The authorized representative in the UK is Bausch & Lomb U.K. Ltd..

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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Phacoemulsification system handpiece

MHRA Device ID: 92150•Ref: 92150

Device Type

General Medical Device

Devices

Phacoemulsification system handpiece

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jan 4, 2024

Manufacturer Information

Name

Bausch & Lomb Incorporated

Address

1400 North Goodman Street

Rochester, New York, United States

Created Date

Feb 18, 2021

Authorized Representative

Name

Bausch & Lomb U.K. Ltd.

Relationship Type

UK Responsible Person

Address

106-114 London Road

Kingston upon Thames, Surrey, England, United Kingdom

Postcode: KT2 6TN

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Phacoemulsification system handpiece - 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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