International safety notice
Argon Medical Devices SuperCore Semi-Automatic Biopsy Instrument - tagasikutsumine, tootmisdefekti tõttu seade ei püsi koos
Estonia / EMDDB · EST · Oct 1, 2021
Key facts
| Title | Argon Medical Devices SuperCore Semi-Automatic Biopsy Instrument - tagasikutsumine, tootmisdefekti tõttu seade ei püsi koos |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Argon Medical Devices SuperCore Semi-Automatic Biopsy Instrument |
| Manufacturer | ARGON MEDICAL DEVICES SUPERCORE SEMIAUTOMATIC BIOPSY INSTRUMENT |
| Models | 11382998, 11362716, 75751, 701214090, 11363320, 11370574, 11378295, 11372366, 11376074, 11375663, 11374807, 11379724 and 66 more |
| Date | Oct 1, 2021 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 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