International safety notice
Technical name: Vital Signs Monitor
Brazil / Anvisa · BRA · Sep 21, 2017
Key facts
| Title | Technical name: Vital Signs Monitor |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Intellivue Patient Monitor Technical name: Vital Signs Monitor ANVISA registration number: 10216710215 Risk class: III Affected model: MX400, MX450, MX500, MX550, MX700, MX800 Numbers of the following series: DE5630GA7B; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 AV TAMBORÉ 14001440 BOX 31 A 33 TAMBORÉ BARUERI SP FABRICANTE PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH HEWLETTPACKARD STRASSE 2 71034 BÖBLINGEN ALEMANHA EMAIL REGULATORIOSPHILIPSCOM |
| Models | DE5630GHLJ, DE5630GHN2, DE5630GA7B, DE5630GHM4, DE5630GHMZ, MX500, DE5630GHMW, DE5630GEC2, DE5630GEBK, DE5630GHLF, DE5630GHKV, MX550 and 39 more |
| Date | Sep 21, 2017 |
| 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