Dermatological laser beam guiding handpiece - UK MHRA Medical Device Registration

Dermatological laser beam guiding handpiece is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99103. The device is manufactured by Cutera, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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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Dermatological laser beam guiding handpiece

MHRA Device ID: 99103•Ref: 99103

Device Type

General Medical Device

Devices

Dermatological laser beam guiding handpiece

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jun 28, 2024

Manufacturer Information

Name

Cutera, Inc.

Address

3240 Bayshore Boulevard

Brisbane, CA, United States

Created Date

Aug 26, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Dermatological laser beam guiding handpiece - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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