Data / Medical devices / China / Chinamed Products (china) Ltd.
Chinamed Products (china) Ltd.: FDA-registered device maker in Gaoyao District Guangdong, China, 2 510(k) clearances
Chinamed Products (china) Ltd. is registered with the FDA (registration 3003799815) in Gaoyao District Guangdong, China. It lists 8 device types. The FDA files 2 510(k) clearances under its listings, the newest dated August 25, 2016. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3003799815
- Address
- Xin Tang Industrial Park Jiao Tang Town, Gaoyao District Guangdong, China, --
- Owner or operator
- CHINAMED PRODUCTS LTD. (9052298)
- Roles
- Manufacturer
- First device listed
- July 27, 2002
- Registered through
- 2026
- Brand names listed
- AirLife
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter And Tip, Suction | JOL | 2 | Manufacturer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Manufacturer | accessdata.fda.gov |
| Connector, Airway (Extension) | BZA | 1 | Manufacturer | accessdata.fda.gov |
| Drain, Tee (Water Trap) | BYH | 1 | Manufacturer | accessdata.fda.gov |
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Manufacturer | accessdata.fda.gov |
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | 2 | Manufacturer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Manufacturer | accessdata.fda.gov |
| Spirometer, Therapeutic (Incentive) | BWF | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 25, 2016 | K160764 | AirLife Autofill Humidification Chamber | BTT | Substantially Equivalent | Carefusion 2200, Inc. | accessdata.fda.gov |
| September 26, 1979 | K791819 | AIR INCENTIVE SPIROMETER | BWF | Substantially Equivalent | Airlife, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheters, Suction, Tracheobronchial
- All makers of Spirometer, Therapeutic (Incentive)
- All makers of Drain, Tee (Water Trap)
- All makers of Humidifier, Respiratory Gas, (Direct Patient Interface)
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Catheter And Tip, Suction
Updated August 25, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.