International safety notice
Anesthesia Systems
Brazil / Anvisa · BRA · Dec 29, 2015
Key facts
| Title | Anesthesia Systems |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Anesthesia Devices (various) ANVISA registration number: Aespire S/5 7900 (Reg. 80071260227), Aespire View (Reg. 80071260133), Aestiva/5 MRI (Reg. 80071260331), Aisys (Reg. 80071260272), Aisys CS2 (Reg. 80071260326 ) and Next CS2 (Reg. 80071260306) and maintenance kit: 1009-8216-000, 1503-3006-000, 1503-8102-000, 1009-8423-000, 1503-8101-000) under the same registrations Risk class: III Model(s) affected; |
| Manufacturer | NOME DA EMPRESA FABRICANTE DATEX OHMEDA INC PAÍS ESTADOS UNIDOS ENDEREÇO 3030 OHMEDA DRIVE MADISONWI |
| Models | 1503-8101-000, 1503-3006-000, 80071260133, 80071260326, 1009-8423-000, 80071260227, 1009-8216-000, 1503-8102-000, 80071260331, 80071260306, 80071260272 |
| Date | Dec 29, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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