International safety notice
No use of RAUMEDIC NEUROVENT-catheters in combination with HP M1006 pressure modules
Germany / BfArM · DEU · Mar 23, 2006
Key facts
| Title | No use of RAUMEDIC NEUROVENT-catheters in combination with HP M1006 pressure modules |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | No use of RAUMEDIC NEUROVENT-catheters in combination with HP M1006 pressure modules |
| Manufacturer | No use of RAUMEDIC NEUROVENT-catheters in combination with HP M1006 pressure modules |
| Models | NPS-2, DS-8000, 78341, 78346, 78342, D-95205, 6802XL, HS-500, 27.1.1, 78352, DS-110, DS-5300W and 25 more |
| Date | Mar 23, 2006 |
| Regulator page | bfarm.de |
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