Data / Medical devices / Multiple Use Blood Lancet For Single Patient Use Only / Taiwan
FDA-registered makers of Multiple Use Blood Lancet For Single Patient Use Only in Taiwan: 5 establishments
5 establishments in Taiwan are registered with the FDA to make Multiple Use Blood Lancet For Single Patient Use Only (product code QRL). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Multiple Use Blood Lancet For Single Patient Use Only
- Product code
- QRL
- Country
- Taiwan
Makers of Multiple Use Blood Lancet For Single Patient Use Only in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bionime Corporation | Taichung City, Taiwan | Manufacturer | 1 | September 26, 2022 | 0 | 0 | 0 | api.fda.gov |
| Gostar Co., Ltd. | New Taipei City, Taiwan | Specification developer | 1 | January 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| Taidoc Technology Corporation | New Taipei City, Taiwan | Manufacturer | 1 | January 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| Alliance International Medical Co., Ltd. | New Taipei City, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medifun Corporation | Taichung, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.