Procainamide therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

Procainamide therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207723. The device is manufactured by Siemens Healthcare Diagnostics Inc from United States, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Procainamide therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry

MHRA Device ID: 207723

Device Type

In Vitro Diagnostic Device

Type

Class C

Status

DREGIY

Date Registered

Dec 25, 2024

Manufacturer Information

Name

Siemens Healthcare Diagnostics Inc

Address

511 Benedict Avenue

Tarrytown, NY, United States

DJ Fang

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Procainamide therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

Device Type

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Status

Date Registered

Name

Address

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