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ProImplant

EUDAMED

Class IIb (EU MDR)

Ref 5102.3Model ProImplant D2.1/L7Ref 6102.3Model ProImplant D2.1/L10Ref 7102.3Model ProImplant D2.1/L14

by LASAK s.r.o.

Identity

Trade Name
ProImplant EUDAMED
Device Name
ProImplant EUDAMED
Model / Reference
ProImplant D2.1/L7 EUDAMED
5102.3 EUDAMED
ProImplant D2.1/L10 EUDAMED
6102.3 EUDAMED
ProImplant D2.1/L14 EUDAMED
7102.3 EUDAMED

Identifiers

Primary DI / UDI-DI
08595573019426 EUDAMED
08595573019440 EUDAMED
08595573019464 EUDAMED
Basic UDI-DI
B-08595573019426 EUDAMED
B-08595573019440 EUDAMED
B-08595573019464 EUDAMED
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

ProImplant by LASAK s.r.o. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
LASAK s.r.o.
EUDAMED SRN
CZ-MF-000031907

Sources (3)

  • EUDAMED 40fc30ce-cd39-4812-8a9f-2c752dac161a 61 fields · synced Aug 4, 2026
  • EUDAMED 9089b502-f19a-4cfb-9a8c-746e12124404 61 fields · synced May 17, 2026
  • EUDAMED 35f15a82-0d44-442f-8761-2b0872351b06 61 fields · synced May 19, 2026