International safety notice
RESPIRATORS RESPIRATORS, INTENSIVE CARE, ADULT RESPIRATORS, INTENSIVE CARE, ADULT RESPIRATORS, INTENSIVE/NEONATAL CARE
Brazil / Anvisa · BRA · Jun 2, 2000
Key facts
| Title | RESPIRATORS RESPIRATORS, INTENSIVE CARE, ADULT RESPIRATORS, INTENSIVE CARE, ADULT RESPIRATORS, INTENSIVE/NEONATAL CARE |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ADULT/PEDIATRIC RESPIRATORS MODEL 1000 BEAR; |
| Manufacturer | BEAR MEDICAL SYSTEMS INC SUB THERMO ELECTRON CORP 101095 1100 BIRD CENTER DR PALM SPRINGS CA 92262 |
| Models | 50-08555, 50-08550, 11008959, 50-08570, 50-08560, 11008756 |
| Date | Jun 2, 2000 |
| 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