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V. Mueller

CAREFUSION 2200, INC · Model 006.06 · UDI-DI 10885403067532

HMW Prescription
1
510(k) clearances
7
Adverse events
0
Recalls
25
Facilities

Description

LASER CAMERA DRAPE 6IN X96IN 25/BX

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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.