Data / Medical devices / China / Qingdao Traworks Co., Ltd.
Qingdao Traworks Co., Ltd.: FDA-registered device maker in QINGDAO Shandong, China, 1 510(k) clearance
Qingdao Traworks Co., Ltd. is registered with the FDA (registration 3004527595) in QINGDAO Shandong, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 18, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004527595
- Address
- 15 Donghai Road West Inter Royal Building 16G, QINGDAO Shandong, China, 266071
- Owner or operator
- Qingdao TraWorks Co., Ltd (9072957)
- Roles
- Exporter to the US
- First device listed
- May 10, 2005
- Registered through
- 2026
- Brand names listed
- ET Tubes, Intubating Stylet, LARYNGEAL MASK AIRWAY(LMA), Nasopharyngeal Tube, STETHOSCOPES, Specimen Container, Urine Collector
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Airway, Nasopharyngeal | BTQ | 1 | Exporter to the US | accessdata.fda.gov |
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Exporter to the US | accessdata.fda.gov |
| Collector, Urine, Powered, Non Indwelling Catheter | NZU | 1 | Exporter to the US | accessdata.fda.gov |
| Container, Specimen, Non-Sterile | NNI | 1 | Exporter to the US | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Exporter to the US | accessdata.fda.gov |
| Stylet, Tracheal Tube | BSR | 1 | Exporter to the US | accessdata.fda.gov |
| Tube, Tracheal (W/Wo Connector) | BTR | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| February 18, 2005 | K042683 | WELL LEAD ENDOTRACHEAL TUBE | BTR | Substantially Equivalent | Well Lead Medical Instruments | accessdata.fda.gov |
Compare with other makers
- All makers of Airway, Nasopharyngeal
- All makers of Stethoscope, Manual
- All makers of Airway, Oropharyngeal, Anesthesiology
- All makers of Container, Specimen, Non-Sterile
- All makers of Collector, Urine, Powered, Non Indwelling Catheter
- All makers of Tube, Tracheal (W/Wo Connector)
Updated February 18, 2005. 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.