Sputum specimen liquefaction/decontamination kit IVD - UK MHRA Medical Device Registration

Sputum specimen liquefaction/decontamination kit IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 139279. The device is manufactured by Alpha-Tec Systems, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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Sputum specimen liquefaction/decontamination kit IVD

MHRA Device ID: 139279•Ref: 139279

Device Type

In Vitro Diagnostic Device

Devices

Sputum specimen liquefaction/decontamination kit IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2023

Manufacturer Information

Name

Alpha-Tec Systems, Inc.

Address

1311 SE Cardinal Court, Suite 170

Vancouver, WA, United States

Created Date

Mar 8, 2022

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Sputum specimen liquefaction/decontamination kit IVD - 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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