International safety notice
RADIOGRAPHIC/FLUOROSCOPIC SYSTEMS, GENERAL USE, DIRECT-CONTROLLED
Brazil / Anvisa · BRA · Oct 20, 2000
Key facts
| Title | RADIOGRAPHIC/FLUOROSCOPIC SYSTEMS, GENERAL USE, DIRECT-CONTROLLED |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | FLUOROSCOPIC X-RAY SYSTEMS WITH MULTI DIAGNOSIS IN AMPLIFIED IMAGE (MULTIDIAGNOST IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEMS): (1) MODEL 3, (2) MODEL 4. ALL SYSTEMS OF THESE MODELS MENTIONED INSTALLED BEFORE MARCH 2000. |
| Manufacturer | PHILIPS MEDICAL SYSTEMS NORTH AMERICA 102120 710 BRIDGEPORT AVE PO BOX 860 SHELTON CT 064840917 DISTRIBUIDOR PHILIPS MEDICAL SYSTEMS NEDERLAND BV 177242 VEENPLUIS 6 POSTBUS 70000 NL5606 DA BEST PAÍSES BAIXOS |
| Date | Oct 20, 2000 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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