Home › Orantech Inc. › Orantech
Orantech
Orantech Inc. · Model BPH-AS15-02M-02M · UDI-DI 06941691961925
10
510(k) clearances
2
Adverse events
1
Recalls
40
Facilities
Description
Bionet Compatible, Adult/Pediatric, Single tube, 1.5m
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-07-20 | Xsensor Technology Corporation | The plastic enclosures for the X3 Display and X3 PRO Pressure Mapping System has a UL94 HB flammability rating while the medical equipment specification UL 60601-1 requires V-2 rat |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
