Nephelometry/turbidimetry analyser IVD, automated/semi-automated - UK MHRA Medical Device Registration

Nephelometry/turbidimetry analyser IVD, automated/semi-automated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 179229. The device is manufactured by Acon Laboratories, 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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In Vitro Diagnostic Device

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Nephelometry/turbidimetry analyser IVD, automated/semi-automated

MHRA Device ID: 179229•Ref: 179229

Device Type

In Vitro Diagnostic Device

Devices

Nephelometry/turbidimetry analyser IVD, automated/semi-automated

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Mar 12, 2024

Manufacturer Information

Name

Acon Laboratories, Inc.

Address

5850 Oberlin Drive, #340

San Diego, CA, United States

Created Date

Mar 31, 2021

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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Nephelometry/turbidimetry analyser IVD, automated/semi-automated - UK MHRA Medical Device Registration

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DJ Fang

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