Patient positioning foam mould kit - UK MHRA Medical Device Registration

Patient positioning foam mould kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138180. The device is manufactured by Medtec LLC dba CIVCO Radiotherapy from United States, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Patient positioning foam mould kit

MHRA Device ID: 138180•Ref: 138180

Device Type

General Medical Device

Devices

Patient positioning foam mould kit

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Medtec LLC dba CIVCO Radiotherapy

Address

1401 8th St SE

Orange City, Iowa, United States

Created Date

Mar 19, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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Patient positioning foam mould kit - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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