FDA Device Intelligence
HomeMEDIMAX TECH INC. › MediMax Tech

MediMax Tech

MEDIMAX TECH INC. · Model BC2530 Needle Electrodes · UDI-DI 00817325020008

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

Description

BC2530 Needle Electrodes - Concentric Needle, Non-Wired, 25mm Length, 0.30mm(30G) Diameter.

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.