Data / Medical devices / China / Ningbo Besmed Medical Equipment Corp.
Ningbo Besmed Medical Equipment Corp.: FDA-registered device maker in NINGBO Zhejiang, China, 3 510(k) clearances
Ningbo Besmed Medical Equipment Corp. is registered with the FDA (registration 3006547005) in NINGBO Zhejiang, China. It lists 13 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 30, 2015. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3006547005
- Address
- No.51, Mo Gan Shan RD, Beilun, NINGBO Zhejiang, China, 315800
- Owner or operator
- BESMED HEALTH BUSINESS CORP. (9047866)
- Roles
- Manufacturer
- First device listed
- June 26, 2007
- Registered through
- 2026
- Brand names listed
- , OXYGEN, AEROSOL, AIR CUSHION MASK, ANESTHESIA BREATHING CIRCUIT, BESMED AIR CUSHION MASK, BESMED ANESTHESIA CIRCUIT, BESMED BERMAN, BESMED BITE BLOCK and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Manufacturer | accessdata.fda.gov |
| Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | CCK | 2 | Manufacturer | accessdata.fda.gov |
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer | accessdata.fda.gov |
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Manufacturer | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Gas, Anesthetic | BSJ | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Oxygen, Non-Rebreathing | KGB | 1 | Manufacturer | accessdata.fda.gov |
| Mouthpiece, Breathing | BYP | 1 | Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| Set, Tubing And Support, Ventilator (W Harness) | BZO | 1 | Manufacturer | accessdata.fda.gov |
| Strap, Head, Gas Mask | BTK | 1 | Manufacturer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 1 | 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 |
|---|---|---|---|---|---|---|
| June 30, 2015 | K150591 | Besmed Reusable Jet Nebulizer | CAF | Substantially Equivalent | Besmed Health Business Corp | accessdata.fda.gov |
| February 5, 2015 | K143150 | CO2 monitoring line with and without in-line filter | CCK | Substantially Equivalent | Besmed Health Business Corp | accessdata.fda.gov |
| November 10, 2009 | K091272 | BESMED JET NEBULIZER BOTTLE SET | CAF | Substantially Equivalent | Besmed Health Business Corp | accessdata.fda.gov |
Compare with other makers
- All makers of Airway, Oropharyngeal, Anesthesiology
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Mouthpiece, Breathing
- All makers of Set, Tubing And Support, Ventilator (W Harness)
- All makers of Strap, Head, Gas Mask
- All makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Updated June 30, 2015. 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.