- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 18, 2026
69509009CEIKRWIS03A is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Shanghai INT Medical Instruments Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0695090092644069509009CEIKRWIS03A(01)06950900926440
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
C0504ARTERIAL INTRODUCTION SETSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market | |
| Austria | Still on market | |
| Belgium | Still on market | |
| Cyprus | Still on market | |
| Denmark | Still on market | |
| Estonia | Still on market | |
| EL | Still on market | |
| Finland | Still on market | |
| Croatia | Still on market | |
| Ireland | Still on market | |
| Latvia | Still on market | |
| Malta | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market |
CN-MF-000009966Certificate health across this manufacturer's portfolio.
3QMS-MDR-0068/06/2025Issued1QMS-MDR-0068/06/2025Issued