International safety notice
Medi-Trace CADENCE - Electrodes for defibrillation - Model: 22660R - Registration: 80136710169 Risk Class I
Brazil / Anvisa · BRA · Oct 20, 2014
Key facts
| Title | Medi-Trace CADENCE - Electrodes for defibrillation - Model: 22660R - Registration: 80136710169 Risk Class I |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Medi-Trace CADENCE - Electrodes for defibrillation - Model: 22660R - Registration: 80136710169 Risk Class I (AFFECTED LOTS ATTACHED) |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL AUTO SUTURE DO BRASIL LTDA AV JORNALISTA ROBERTO MARINHO 85 11º ANDAR CNPJ 01645409000128 SÃO PAULOSP FONE 11 21876457 21876273 EMAIL TECNOVIGILANCIACOVIDIENCOM FABRICANTE LUDLOWA DIVISION OF TYCO HEALTHCARE GROUP LP TWO LUDLOW PARK DRIVE CHICOPE MA EUA |
| Models | 22660R, 80136710169 |
| Date | Oct 20, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1