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EUDAMED last updated this device on Dec 20, 2024
590528981000GHLAP 5 Disposable Endoscopic Atraumatic Fenestrated Grasper is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Konmex Spółka z ograniczoną odpowiedzialnością. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05905289818139590528981000GH0208-DGLAP501B(01)05905289818139
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.
K0201010602LAPAROSCOPIC AND THORACOSCOPIC ELECTROSURGERY FORCEPS, SINGLE-USE5 warnings recorded — scroll inside the panel to see all entries.
CW001CW011CW010CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Jul 15, 2024 | Still on market |
| Belgium | Still on market | |
| EL | Still on market |
PL-MF-000033845Certificate health across this manufacturer's portfolio.
1434-MDR-003/2024Issued590528981000GHOn the marketLAP 5 Disposable Endoscopic Dissector Maryland590528981000GHOn the marketLAP 5 Disposable Endoscopic Dissector Maryland590528981000GHOn the marketLAP 5 Disposable Endoscopic Grasper Allis590528981000GHOn the marketLAP 5 Disposable Endoscopic Grasper Allis590528981000GHOn the market