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Vibrasat Pro Console

Möller Medical GmbH · Model 00003921 · UDI-DI 04260277178055

QPB
1
510(k) clearances
71
Adverse events
1
Recalls
50
Facilities

Description

The vibrating drive system 'Vibrasat Pro' is used to oscillate cannulas to support the hand movement of the user.

Recalls

DateFirmReason
2024-10-18HUMAN MED AGThe cannula tubes do not comply with the specification. The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spra

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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.