Home › Ibramed Industria Brasileira de Equipamentos Medicos Eir › Ibramed

Ibramed

Ibramed Industria Brasileira de Equipamentos Medicos Eir · Model CELLEBRA · UDI-DI 07898961579092

IMI Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

CELLEBRA is a therapeutic ultrasound microcontrolled device in the frequencies of 1 MHz and 3 MHz, designed to be used for physiotherapy treatments.

Recalls

Date	Firm	Reason
2008-02-28	Chattanooga Corp Inc	Device may fail to administer therapy during use.
2008-02-28	Chattanooga Corp Inc	Device may fail to administer therapy during use.
2005-01-05	Sybaritic, Inc	Device is performing functions that are not cleared in the 510(k).

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 key Read 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.