Ophthalmic cannulation set, single-use - UK MHRA Medical Device Registration

Ophthalmic cannulation set, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91831. The device is manufactured by MANI, INC. from Japan, classified as General Medical Device. The authorized representative in the UK is Obelis UK 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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Ophthalmic cannulation set, single-use

MHRA Device ID: 91831•Ref: 91831

Device Type

General Medical Device

Devices

Ophthalmic cannulation set, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Feb 28, 2024

Manufacturer Information

Name

MANI, INC.

Address

8-3 Kiyohara Industrial Park

Utsunomiya, Tochigi, Japan

Created Date

Apr 29, 2021

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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Other Products from MANI, INC. (10)

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Ophthalmic cannulation set, single-use - UK MHRA Medical Device Registration

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Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

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DJ Fang

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