Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003799815

FEI Number

3003799815

Entity Name

CHINAMED PRODUCTS (CHINA) LTD.

City/State/Country

Gaoyao District Guangdong, CN

Establishment Address

Xin Tang Industrial Park, Jiao Tang Town, Gaoyao District Guangdong --, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CHINAMED PRODUCTS LTD. (Owner Number: 9052298)

Owner / Operator Contact Address

Xin Tang Industrial Park, Jiao Tang Town, Gaoyao City, CN-GD 44 526100, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AirLife AirLife AirLife AirLife AirLife AirLife

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYG	Mask, Oxygen	Anesthesiology	Class 1	868.5580	2009-01-06
BYH	Drain, Tee (Water Trap)	Anesthesiology	Class 1	868.5995	2002-07-27
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2013-05-31
JOL	Catheter And Tip, Suction	General Hospital	Class 2	880.6740	2012-12-21
BTT	Humidifier, Respiratory Gas, (Direct Patient Interface)	Anesthesiology	Class 2	868.5450	2016-12-01
BZA	Connector, Airway (Extension)	Anesthesiology	Class 1	868.5810	2002-07-27

Official Correspondent

No official correspondent registered.

US Agent Details

Billy Reece Business: CHINAMED WEST INC. Email: billy@chinamedwest.com Phone: (909) 6484024

Related Public Records

Same Entity

CHINAMED PRODUCTS LTD.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K012633	Respironics, Inc.	RESPIRONICS HEATED HUMIDIFIER	2002-02-28
K970478	Marquest Medical Products, Inc.	SCT 3000 HEATED HUMIDIFIER	1997-07-16

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2013	Invuity, Inc.	2	BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a sterilization tray. The Invuity Brite Field Illuminated Suction Device is intended to aspirate from the surgical site and to provide illumination from a high intensity light source.

Similar Registrations

Registration Number	Establishment Name	Location
3044777184	SAVING STORY CO.,LTD	Hwaseong-si Gyeonggi, KR
3003767629	TECNOLOGIAS MEDICAS INNOVADORAS S DE RL	H. MATAMOROS Tamaulipas, MX
3010272829	Salter Labs de Mexico de S.A. de C.V.	Chihuahua Mexico, MX
3010205626	Globalcare Medical Technology HK, Ltd.	Hong Kong, HK
1043214	DEROYAL INDUSTRIES, INC.	POWELL, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003799815. Last updated year: 2026. Please use registration number 3003799815 when referencing this establishment in official correspondence.