FDA Device Intelligence
Home › Ambu A/S › Neuroline SubdermalNeurology Needle Electrodes

Neuroline SubdermalNeurology Needle Electrodes

Ambu A/S · Model 74512-100/24 · UDI-DI 05707480024162

IKT Prescription
10
510(k) clearances
150
Adverse events
2
Recalls
39
Facilities

Description

Needle Electrode Length: 12 mm (0.5") Leadwire Length: 100 cm (40") Each box of 24 consists of 4 pieces in each of the colors: White, Green, Blue, Yellow, Red, Black

Recalls

DateFirmReason
2022-08-09Technomed EuropeBurns of varying degrees can occur to patients with electrodes left in while in the MRI scanner as a result of inadequate safety information in the IFU.
2007-04-12Chalgren Enterprises IncSterility Compromised-- Investigation found that individual packaging seals were separating, which may compromise sterility.

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.