Phacoemulsification/vitrectomy system - UK MHRA Medical Device Registration

Phacoemulsification/vitrectomy system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92144. 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..

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Phacoemulsification/vitrectomy system

MHRA Device ID: 92144•Ref: 92144

Device Type

General Medical Device

Devices

Phacoemulsification/vitrectomy system

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/vitrectomy system - UK MHRA Medical Device Registration

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Phacoemulsification/vitrectomy system