Mechanical pipette - UK MHRA Medical Device Registration

Mechanical pipette is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89753. The device is manufactured by Sunlight Medical Inc from United States, classified as General Medical Device. The authorized representative in the UK is Fujifilm Healthcare UK 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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General Medical Device

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Mechanical pipette

MHRA Device ID: 89753•Ref: 89753

Device Type

General Medical Device

Devices

Mechanical pipette

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

Sunlight Medical Inc

Address

5570 Florida Mining Blvd Suite 603 5570 Florida Mining Blvd

Jacksonville, Florida, United States

Created Date

Jul 21, 2021

Authorized Representative

Name

Fujifilm Healthcare UK Limited

Relationship Type

UK Responsible Person

Address

Fujifilm House Whitbread Way

Bedford, England, United Kingdom

Postcode: MK42 0ZE

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Mechanical pipette - UK MHRA Medical Device Registration

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