United Kingdom MHRA device registration 90469

Glucose IVD, control

United Kingdom·In Vitro Diagnostic Device·VivaChek Biotech (Hangzhou) Co., Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 90469
MHRA Reference Number: 90469
Date Registered: Nov 26, 2024
Last Updated: Jun 11, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Glucose IVD, control
Type: IVD Annex II List B

Manufacturer

Name: VivaChek Biotech (Hangzhou) Co., Ltd.
Address: Level 2, Block 2, 146 East Chaofeng Rd., Yuhang Economy Development Zone,
Hangzhou, Zhejiang, China
Created Date: Mar 14, 2021

Authorized Representative

Name: lotus global co ltd
Relationship Type: UK Responsible Person
Address: 23 Maine Street
Reading, Reading, England, United Kingdom
Postcode: RG2 6AG

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Additional devices represented by lotus global co ltd in the UK

Alpha-fetoprotein (AFP) IVD, kit, fluorescent immunoassayNov 26, 2024

Type: In Vitro Diagnostic Device

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Device ID: 160859

Anti-Mullerian hormone (AMH) IVD, reagentNov 26, 2024

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Cystatin C IVD, reagentNov 26, 2024

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Faecal occult blood IVD, reagentNov 26, 2024

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Follicle stimulating hormone (FSH) IVD, reagentNov 26, 2024

Type: In Vitro Diagnostic Device

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Device ID: 160852

Free triiodothyronine (FT3) IVD, reagentNov 26, 2024

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Haemoglobin detection IVD, controlNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: VivaChek Biotech (Hangzhou) Co., Ltd.

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Glucose IVD, reagentNov 26, 2024

Type: In Vitro Diagnostic Device

Manufacturer: VivaChek Biotech (Hangzhou) Co., Ltd.

Device ID: 90468

About this record

Glucose IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 90469. The device is manufactured by VivaChek Biotech (Hangzhou) Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is lotus global co ltd.

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