International safety notice
Arcuate Aortic Cannula
Brazil / Anvisa · BRA · Mar 6, 2001
Key facts
| Title | Arcuate Aortic Cannula |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Sarns Aortic Arch Cannulae with 3/8-inch connectors: (1) 6.5 mm, (2) 8 mm 24 Fr Flexible, (3) 6.5 mm 20 Fr High Flow with Suture Flange and Luer Port, (4) 24 Fr Wire-Reinforced Flex with Luer Port; |
| Manufacturer | TERUMO CARDIOVASCULAR SYSTEMS CORP DIV TERUMO MEDICAL CORP 371199 6200 JACKSON RD ANN ARBOR MI 48103 |
| Models | 98-0702-0710-9, 15495, 98-0702-1286-9, W507618, 236148, 8-polegadas, W507538, W50743, 241991, 236511, 238279, 236153 and 2 more |
| Date | Mar 6, 2001 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 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