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 Number: 3009077131
• FEI Number: 3009077131
• Name: Marco Mu
• Owner & Operator: Shanghai Kohope Medical Devices Co., Ltd
• Contact Address: 1001, Building 2, Lane 2888 South QIlianshan Road; SHANGHAI CN-31 Shanghai 200333 CN
• Official Correspondent:
  • charlie wang
  • 86-21-60836358-x
• US Agent:
  • Marco Mu
  • MID-LINK INTERNATIONAL CO., LTD
  • 360 3257028
  • 360 9253199
  • us.agent@mid-link.net
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2219 Rimland Dr. Suite 301 ; Bellingham, WA 98226 US
• Establishment Type: Sterilize Medical Device for Another Party (Contract Sterilizer)

FDA Filings

Device Company	Device	Date
PMN K190002 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 Use	2019-09-12
PMN K112057 | FMI Marco Mu [Shanghai Kohope Medical Devices Co., Ltd]	PISTON SYRINGE	2016-04-28
PMN K112057 | FMF Marco Mu [Shanghai Kohope Medical Devices Co., Ltd]	PISTON SYRINGE	2016-04-28