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Algiloid

EUDAMED

Class I (EU MDR)

Ref 101401Model 000400

by Hager & Werken GmbH & Co. KG

Identity

Trade Name
Algiloid EUDAMED
Device Name
Abformmaterial, dental EUDAMED
Model / Reference
000400 EUDAMED
101401 EUDAMED

Identifiers

Primary DI / UDI-DI
04099637003252 EUDAMED
Basic UDI-DI
40996370004003J EUDAMED
Unit of Use DI
04099637003245 EUDAMED
EMDN Code
Q01020199 DENTAL IMPRESSION MATERIALS - OTHER 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: Silicone dental impression material

Algiloid by Hager & Werken GmbH & Co. KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

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 d180130b-30a6-4f74-ae1c-9bab26a1d01d 61 fields · synced Jul 10, 2026