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iSy® Impression post

EUDAMED

Class I (EU MDR)

Ref P2110.0001

by ALTATEC GmbH

Identity

Trade Name
iSy® Impression post EUDAMED
Device Name
iSy® Impression post, closed tray EUDAMED
Model / Reference
P2110.0001 EUDAMED

Identifiers

Primary DI / UDI-DI
04099797020618 EUDAMED
Basic UDI-DI
40997970008120000000000KC EUDAMED
Secondary DI
E219P211000011 EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES 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

iSy® Impression post by ALTATEC GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (1)

  • EUDAMED 7c354816-ae85-4d8f-a297-7e897e24e994 61 fields · synced May 22, 2026