Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “Lanko”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 6 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 6

More countries (1)

Czechia 6

Risk class Class I 6 Class IIa Class IIb Class III Class II (US)

More classes (11)

Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

Verified Verified only

Category (EMDN)

Browse by category

6 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Lanko UDI-DI 08595719432324

Pavel Plašil,Czechia

Active Regimes: CE MDD Registry: EUDAMED Class:I
3 variants
- Lanko PL1956
- Lanko PL1976
Lanko prodlužovací

Pavel Plašil,Czechia

Active Regimes: CE MDD Registry: EUDAMED Class:I
Lanko + koncovky striptorů UDI-DI 08595719432256

Pavel Plašil,Czechia

Active Regimes: CE MDD Registry: EUDAMED Class:I
2 variants
- Lanko + koncovky striptorů PL0151

Previous Next

Showing 1-6 of 6

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site