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Algilock Perforiert OK / PS 4

EUDAMED

Class I (EU MDR)

Ref 101032Model 000100

by Hager & Werken GmbH & Co. KG

Identity

Trade Name
Algilock Perforiert OK / PS 4 EUDAMED
Device Name
Abformlöffel, wiederaufbereitbar EUDAMED
Model / Reference
000100 EUDAMED
101032 EUDAMED

Identifiers

Primary DI / UDI-DI
04099637002323 EUDAMED
Basic UDI-DI
409963700010033 EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Algilock Perforiert OK / PS 4 by Hager & Werken GmbH & Co. KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000004938

Sources (1)

  • EUDAMED 69272ea8-1936-4c0d-98de-e82f0c72d661 61 fields · synced Jun 18, 2026