International safety notice
Technical name: AUTOMATIC / SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR
Brazil / Anvisa · BRA · Nov 16, 2016
Key facts
| Title | Technical name: AUTOMATIC / SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: NIHON KOHDEN AUTOMATIC EXTERNAL DEFIBRILLATOR Technical name: AUTOMATIC / SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR ANVISA registration number: 80117580147 Risk class: III Affected model: CARDIOLIFE AED 2100K Affected serial numbers: Serial numbers: 10462, 10463, 10464 , 10465, 10466, 10467, 10468, 10469, 10470, 10471, 11588, 11589, 11590, 11591, 11592, 11593, 11594, 11596, 11597, 11599, 11 600, 11601, 11602, 11603 and 11604 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO EMERGO BRAZIL IMPORT IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDA ENDEREÇO SIA TRECHO 3 LOTES 20102020 1 ANDAR ED MYRIAM BAIRRO ZONA INDUSTRIAL DF TEL 6133863166 FABRICANTE NIHON KOHDEN TOMIOKA CORPORATION PAÍS JAPÃO |
| Models | 11603, 11593, 11604, 11590, 11594, 11599, 11601, 10469, 10466, 80117580147, 11596, 10468 and 15 more |
| Date | Nov 16, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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