Potassium (K+) electrode IVD - UK MHRA Medical Device Registration

Potassium (K+) electrode IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 3739. The device is manufactured by Siemens Healthcare Diagnostics Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Siemens Healthcare Diagnostics Limited.

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Potassium (K+) electrode IVD

MHRA Device ID: 3739•Ref: 3739

Device Type

In Vitro Diagnostic Device

Devices

Potassium (K+) electrode IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 16, 2024

Manufacturer Information

Name

Siemens Healthcare Diagnostics Inc

Address

511 Benedict Avenue

Tarrytown, NY, United States

Created Date

Oct 19, 2017

Authorized Representative

Name

Siemens Healthcare Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Park View Watchmoor Park

Surrey, Camberley, England, United Kingdom

Postcode: GU15 3YL

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Potassium (K+) electrode IVD - UK MHRA Medical Device Registration

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