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AESCULAP

Aesculap AG · Model FK899R · UDI-DI 04046963150815

HAD Prescription
3
510(k) clearances
43
Adverse events
0
Recalls
3
Facilities

Description

KAIRISON Handle pneumatic, non-sterile, reusable, to be used with: FK881R, FK882R, FK883R, FK884R, FK885R, FK894R, FK895R

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.