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PLS IMPLADENT – impression post

by LASAK s.r.o. EUDAMED

Active European Union

Ref 950002BModel Closed Tray Impression Post; Fastening Screw; Impres. Abut. Cop.; Impression Coping; Open Tray Impression Post; PLS IMPLADENT; ProImplant titanium coping, Scanbody IMPLADENT; Space Maintainer; Space ring

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number85955730032XV Basic UDI-DIDate23 Jun 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
IMPLADENT Impression and Laboratory Components
Model / Reference
Closed Tray Impression Post, Fastening Screw, Impres. Abut. Cop., Impression Coping, Open Tray Impression Post, PLS IMPLADENT, ProImplant titanium coping, Scanbody IMPLADENT, Space Maintainer, Space ring, 950002B
Primary DI / UDI-DI
08595573001193
Basic UDI-DI
85955730032XV
EMDN Code
Q010207 Dental impression devices for prosthetic dentistry
Device Class
Class I
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000031907

Related devices

Category: Dental implant suprastructure, temporary, preformed, single-use

Other devices from LASAK s.r.o.

See all devices from LASAK s.r.o. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No