Aikang Medtech Co L T D

FDA Filings

This page includes the latest FDA filings for Aikang Medtech Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3010402964
FEI Number3010402964
NameAIKANG MEDTECH CO.,LTD
Owner & OperatorAikang MedTech Co.,Ltd
Contact Address501-A08,Bldg.B,Shenfubao Modern Optics P
Shenzhen CN-44 Guangdong 518131 CN
Official Correspondent
  • Chuanguo Zhang
  • 086-755-23035719-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address501-A08,Bldg.B,Shenfubao Modern Optics Plant Area,No.14,Jinxiu M
Shenzhen Guangdong, 518131 CN
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
AIKANG MEDTECH CO.,LTD
Nucleic Acid extracting system2015-10-09
AIKANG MEDTECH CO.,LTD
Automated liquid handling system : Uranus series, Xanuts series2015-10-09
AIKANG MEDTECH CO.,LTD
Automated blood component separator2015-10-09
AIKANG MEDTECH CO.,LTD
Plasma Freezers : Oceanus series2015-10-09
AIKANG MEDTECH CO.,LTD
Large capacity refrigerated centrifuge2015-10-09
AIKANG MEDTECH CO.,LTD
High speed refrigerated centrifuge2015-10-09
AIKANG MEDTECH CO.,LTD
High speed centrifuge2015-10-09
AIKANG MEDTECH CO.,LTD
Automated Chemiluminescence Immunoassay System : Tethys series2013-05-16
AIKANG MEDTECH CO.,LTD
Auto Elisa Analyzer : URANUS series2013-05-16
AIKANG MEDTECH CO.,LTD
Automatic Blood Grouping Analyzer : Metis series, Aigel series2013-05-16

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