Shanghai Kohope Medical Devices Co L T D

FDA Filings

This page includes the latest FDA filings for Shanghai Kohope Medical Devices 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 Number3009077131
FEI Number3009077131
NameMarco Mu
Owner & OperatorShanghai Kohope Medical Devices Co., Ltd
Contact Address1001, Building 2, Lane 2888 South QIlianshan Road
SHANGHAI CN-31 Shanghai 200333 CN
Official Correspondent
  • charlie wang
  • 86-21-60836358-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2219 Rimland Dr. Suite 301
Bellingham, WA 98226 US
Establishment TypeSterilize Medical Device for Another Party (Contract Sterilizer)



FDA Filings

Device
Company
DeviceDate
Shanghai Kohope Medical Devices Co., Ltd
Sterile Hypodermic Syringe For Single Use, With/without Needle, Sterile Insulin Syringe For Single Use, With Needle, Sterile Hypodermic Needle For Single Use2019-09-12
Marco Mu [Shanghai Kohope Medical Devices Co., Ltd]
PISTON SYRINGE2016-04-28
Marco Mu [Shanghai Kohope Medical Devices Co., Ltd]
PISTON SYRINGE2016-04-28

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