BEIJING GENESEE BIOTECH, INC.

FDA Device Registration & Listing · BEIJING, CN · Registration 3005450604

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
3005450604
FEI Number
3005450604
Entity Name
BEIJING GENESEE BIOTECH, INC.
City/State/Country
BEIJING, CN
Establishment Address
No. 36, Yanqi Donger Road, Huairou Yanqi Industrial Development Zone, BEIJING 101407, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BEIJING GENESEE BIOTECH, INC. (Owner Number: 9079448)
Owner / Operator Contact Address
yanqi pioneering center 3ed floor, huairou yanqi industrial development zon, Beijing, CN-NOTA 101407, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

OnSite Rapid Test OnSite Rapid Test OnSite Rapid Test

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JSY Kit, Identification, Mycobacteria Microbiology Class 1 866.2660 2008-07-14
GRY Antigens, All, Leptospira Spp. Microbiology Class 2 866.3350 2008-03-10
GRM Antisera, All Groups, Salmonella Spp. Microbiology Class 2 866.3550 2008-03-10

Official Correspondent

No official correspondent registered.

US Agent Details

Jerry Zhang Business: CTK Biotech Inc. Email: ra@ctkbiotech.com Phone: (858) 4578698

Related Public Records

Same Entity

BEIJING GENESEE BIOTECH, INC.
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 3005450604. Last updated year: 2026. Please use registration number 3005450604 when referencing this establishment in official correspondence.
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