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Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD - UK MHRA Medical Device Registration

Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 177261. The device is manufactured by KABE-Labortechnik GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL 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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In Vitro Diagnostic Device
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Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD
MHRA Device ID: 177261โ€ขRef: 177261

Device Type

In Vitro Diagnostic Device

Devices

Non-evacuated erythrocyte sedimentation rate (ESR) tube IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

May 25, 2024

Manufacturer Information

Address

JรคgerhofstraรŸe 17

Nรผmbrecht-Elsenroth, North Rhine-Westphalia, Germany

Created Date

Aug 8, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

2 St Andrews Place

Lewes, East Sussex, England, United Kingdom

Postcode: BN7 1UP

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