International safety notice
Zimmer Biomet Pulsavac Plus, Plus AC Wound Debridement System - tagasikutsumine, otsiku luku paigast nihkumine, otsiku ja luku korpuse küljest ära tulemine
Estonia / EMDDB · EST · Jul 1, 2019
Key facts
| Title | Zimmer Biomet Pulsavac Plus, Plus AC Wound Debridement System - tagasikutsumine, otsiku luku paigast nihkumine, otsiku ja luku korpuse küljest ära tulemine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Zimmer Biomet Pulsavac Plus, Plus AC Wound Debridement System |
| Manufacturer | ZIMMER BIOMET PULSAVAC PLUS PLUS AC WOUND DEBRIDEMENT SYSTEM |
| Models | 30492170, Z000012268, 30320496, 29370092, V02591, 29370086, Z000012505, 28863700, 29370088, 30871942, 29637550, 30296156 and 85 more |
| Date | Jul 1, 2019 |
| Regulator page | terviseamet.ee |
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