Blood/fluid warmer air/foam detector - UK MHRA Medical Device Registration

Blood/fluid warmer air/foam detector is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 104475. The device is manufactured by The Surgical Company International B.V. from Netherlands, classified as System or Procedure Pack. 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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Blood/fluid warmer air/foam detector

MHRA Device ID: 104475•Ref: 104475

Device Type

System or Procedure Pack

Devices

Blood/fluid warmer air/foam detector

Type

System or Procedure Pack

Date Registered

Nov 26, 2024

Last Updated

Nov 1, 2024

Manufacturer Information

Name

The Surgical Company International B.V.

Address

Beeldschermweg 6F

Amersfoort, Utrecht, Netherlands

Created Date

Sep 17, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Blood/fluid warmer air/foam detector - 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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