United Kingdom MHRA device registration 160389
Urea IVD, reagent
United Kingdom·In Vitro Diagnostic Device·Zhejiang PushKang Biotechnology Co., Ltd.·Registered Oct 29, 2024Registration details
- Device ID
- 160389
- MHRA Reference Number
- 160389
- Date Registered
- Oct 29, 2024
- Last Updated
- Oct 8, 2023
Device classification
- Device Type
- In Vitro Diagnostic Device
- Devices
- Urea IVD, reagent
- Type
- IVD General
Manufacturer
- Address
- C408, Science and Technology Innovation Park No. 398, Mahuan Road, Binhai New Area, Shaoxing Zhejiang Province, China
- Created Date
- Nov 11, 2022
Authorized Representative
- Relationship Type
- UK Responsible Person
- Address
- 3rd Floor, 70 Gracechurch Street London, England, United KingdomPostcode: EC3V 0HR
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About this record
Urea IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160389. The device is manufactured by Zhejiang PushKang Biotechnology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.
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