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Neurologica
TIDI PRODUCTS, LLC · Model 30020F · UDI-DI 00618125183524
IWY
Prescription
10
510(k) clearances
17
Adverse events (2 deaths)
1
Recalls
28
Facilities
Description
BOARD, HEAD & NECK ENT TABLE, 1 Each
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-06-05 | Brainlab AG | Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings a |
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Get your free API keyRead the docsData 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.