Data / Medical devices / China / Tianjin Hanaco Medical Co.,ltd.
Tianjin Hanaco Medical Co.,ltd.: FDA-registered device maker in Tianjin, China, 1 510(k) clearance
Tianjin Hanaco Medical Co.,ltd. is registered with the FDA (registration 9680448) in Tianjin, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 2, 2000. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 9680448
- FEI number
- 3003886545
- Address
- No. 129 DONGTING RD., TEDA, Tianjin, China, 300457
- Owner or operator
- TIANJIN HANACO MEDICAL CO.,LTD. (9009141)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- May 2, 2012
- Registered through
- 2026
- Brand names listed
- Henry Schein Safety Blood Collection Needle (w/needle cap), Phoenix, SOL-CARE Safety Blood Collection Needle, SOL-CARE Safety Blood Collection Needle (US market, w/needle cap), SOL-CARE Safety Blood Collection Needle w/Pre-attached Holder, SOL-CARE Safety Winged Infusion Set, VACUETTE SAFETY Winged Set+Holder, VACUETTE SAFETY Winged Set+Luer Adapter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Conduction, Anesthetic (W/Wo Introducer) | BSP | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Contract manufacturer | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Contract 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 2, 2000 | K990519 | PHOENIX EPIDURAL & SPINAL NEEDLES | BSP | Substantially Equivalent | Myco Medical Supplies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Conduction, Anesthetic (W/Wo Introducer)
- All makers of Set, Administration, Intravascular
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
Updated June 2, 2000. 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.