FDA Device Intelligence
Home › Aesculap AG › SENSATION

SENSATION

Aesculap AG · Model FM168R · UDI-DI 04046963397166

GZX Prescription
10
510(k) clearances
67
Adverse events (1 deaths)
1
Recalls
137
Facilities

Description

SENSATION Micro scissors, angled left, 45 °, 8 1/2", (215 mm), working length: 3 1/2", (90 mm), bayonet-shaped, sharp/sharp, round plastic handle, blue, non-sterile, reusable

Recalls

DateFirmReason
2007-01-22Medtronic Xomed, Inc.A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The outside box label correctly ind

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 docs
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.