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BodiTrak

Vista Medical Ltd · Model BT2-1616-205 · UDI-DI 07540150600482

JFC
10
510(k) clearances
2
Adverse events
1
Recalls
40
Facilities

Description

seat

Recalls

DateFirmReason
2009-07-20Xsensor Technology CorporationThe 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

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Data 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.