Amniotic membrane perforator, single-use - UK MHRA Medical Device Registration

Amniotic membrane perforator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169537. The device is manufactured by Cetro Medical AB from Sweden, classified as General Medical Device. The authorized representative in the UK is International Associates 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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Amniotic membrane perforator, single-use

MHRA Device ID: 169537•Ref: 169537

Device Type

General Medical Device

Devices

Amniotic membrane perforator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 17, 2024

Manufacturer Information

Name

Cetro Medical AB

Address

Nitgatan 11

Smalandsstenar, Sweden

Created Date

Jan 15, 2022

Authorized Representative

Name

International Associates Limited

Relationship Type

UK Responsible Person

Address

38 Queen Street

Glasgow, Scotland, United Kingdom

Postcode: G1 3DX

DJ Fang

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Other Products from Cetro Medical AB (4)

Other Products from Same Authorized Representative (10)

Amniotic membrane perforator, single-use - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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