JIASHAN YINGJIE ELECTRON CO LTD

FDA Device Registration & Listing · Jiashan Zhejiang, CN · Registration 3006973688

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
3006973688
FEI Number
3006973688
Entity Name
JIASHAN YINGJIE ELECTRON CO LTD
City/State/Country
Jiashan Zhejiang, CN
Establishment Address
No 38 Yexing West Rd Ganyao Town, Jiashan Zhejiang 314100, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Suzhou Exceed BioMed Technology Co., Ltd. (Owner Number: 10058962)
Owner / Operator Contact Address
Room 9o4-2,HuaFu building,No.18,ShiShan Road, SuZhou Hi-tech Park, Suzhou, CN-JS 215011, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TEST TUBE AGGLUTINATION VIEWER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IBJ Light, Microscope Pathology Class 1 864.3600 2018-11-15

Official Correspondent

Yade Yang

US Agent Details

James H LIao Email: james@sino2us.com Phone: (310) 3758169

Related Public Records

Same Entity

Suzhou Exceed BioMed Technology Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3010367859 Evident GuangZhou Co., Ltd. Guangzhou Guangdong, CN
3013395426 NANJING JIANGNAN NOVEL OPTICS CO., LTD. Nanjing Jiangsu, CN
3032109 Gynex Corporation North Richland Hills, TX, US
9614084 MEDICAL DEVICES (PVT) LTD. Sialkot Punjab, PK
1648557 TRANSLITE SUGAR LAND, TX, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006973688. Last updated year: 2026. Please use registration number 3006973688 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.