Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009514517

FEI Number

3009514517

Entity Name

WUHAN CHENKANG SCIENCE TECHNOLOGY CO., LTD

City/State/Country

Wuhan Hubei, CN

Establishment Address

Room 02, Floor 3, Unit 2, Building 23, Wuhan Optical Valley International Biomedical Accelerator, Phase 1.2, the 2nd High-Tech Road 388, East Lake New Technology Development Zone, Wuhan Hubei, Wuhan Hubei 430071, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Wuhan Chenkang Science Technology Co., LTD (Owner Number: 10039309)

Owner / Operator Contact Address

Room 02, Floor 3, Unit 2, Building 23,Ea, st Lake New Technology Development Zone, Wuhan, CN-HB 430071, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

URC Test Reagent for 5-Hydroxyindole Acetic Acid

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CDA	Acid, Nitrous And Nitrosonaphthol, 5-Hydroxyindole Acetic Acid/Serotonin	Clinical Chemistry	Class 1	862.1390	2011-12-24

Official Correspondent

boyle Wang

US Agent Details

hui hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (509) 5816099

Related Public Records

Same Entity

Wuhan Chenkang Science Technology Co., LTD

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009514517. Last updated year: 2026. Please use registration number 3009514517 when referencing this establishment in official correspondence.