Data / Medical devices / Taiwan / VADI Medical Technology Co., Ltd.
VADI Medical Technology Co., Ltd.: FDA-registered device maker in Taoyuan City, Taiwan, 1 510(k) clearance
VADI Medical Technology Co., Ltd. is registered with the FDA (registration 9616445) in Taoyuan City, Taiwan. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 30, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9616445
- FEI number
- 3005749238
- Address
- No.198, Lane 298, Huandong Road, Zhongshan Village Yangmei District, Taoyuan City, Taiwan, 32665
- Owner or operator
- VADI Medical Technology Co., Ltd. (9040244)
- Roles
- Manufacturer
- First device listed
- January 27, 2000
- Registered through
- 2026
- Brand names listed
- ANESTHETIC, Air Way, Airway Connector, Artificial Nose, GAS, Resuscitator, VADI, VADI NASAL CANNULA and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Manufacturer | accessdata.fda.gov |
| Bag, Reservoir | BTC | 1 | 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 |
| Condenser, Heat And Moisture (Artificial Nose) | BYD | 1 | Manufacturer | accessdata.fda.gov |
| Connector, Airway (Extension) | BZA | 1 | Manufacturer | accessdata.fda.gov |
| Drain, Tee (Water Trap) | BYH | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Gas, Anesthetic | BSJ | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Manufacturer | accessdata.fda.gov |
| Set, Tubing And Support, Ventilator (W Harness) | BZO | 1 | Manufacturer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Heating, Powered | IRQ | 1 | Manufacturer | accessdata.fda.gov |
| Ventilator, Emergency, Manual (Resuscitator) | BTM | 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 |
|---|---|---|---|---|---|---|
| January 30, 2004 | K030864 | VADI MANUAL RESUSCITATOR | BTM | Substantially Equivalent | Vedi Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Condenser, Heat And Moisture (Artificial Nose)
- All makers of Set, Tubing And Support, Ventilator (W Harness)
- All makers of Circuit, Breathing (W Connector, Adaptor, Y Piece)
- All makers of Unit, Heating, Powered
- All makers of Ventilator, Emergency, Manual (Resuscitator)
- All makers of Drain, Tee (Water Trap)
Updated January 30, 2004. 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.