International safety notice
In-Ka Ureteral balloon dilatation catheter kit
Spain / AEMPS · ESP · Oct 10, 2022
Key facts
| Title | In-Ka Ureteral balloon dilatation catheter kit |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | In-Ka Ureteral balloon dilatation catheter kit |
| Manufacturer | Coloplast A/S |
| Models | 8214780, 7423916, 7370454, 8419827, 7550875, 7532594, 7925971, 7300136, 8189449, 8046731, 8404248, 7539415 and 84 more |
| Event type | Safety Notice |
| Date | Oct 10, 2022 |
At a glance
- No Recall
- Yes 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