SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD

FDA Device Registration & Listing · SHANGHAI, CN · Registration 3009077131

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009077131
FEI Number
3009077131
Entity Name
SHANGHAI KOHOPE MEDICAL DEVICES CO., LTD
City/State/Country
SHANGHAI, CN
Establishment Address
1001, Building 2, Lane 2888, South QIlianshan Road, SHANGHAI 200333, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shanghai Kohope Medical Devices Co., Ltd (Owner Number: 10051744)
Owner / Operator Contact Address
1001, Building 2, Lane 2888, South QIlianshan Road, SHANGHAI, CN-SH 200333, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

syringe connector

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GCD Connector, Catheter General, Plastic Surgery Class 1 878.4200 2022-03-22

Official Correspondent

charlie wang

US Agent Details

Marco Mu Business: MID-LINK INTERNATIONAL CO., LTD Email: us.agent@mid-link.net Phone: (702) 2095185

Related Public Records

Same Entity

Shanghai Kohope Medical Devices Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009077131. Last updated year: 2026. Please use registration number 3009077131 when referencing this establishment in official correspondence.
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