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IPS e.max CAD CEREC/inLab HT A1 I12/5

EUDAMED

Class IIa (EU MDR)

Ref 626391

by Ivoclar Vivadent AG

Identity

Trade Name
IPS e.max CAD CEREC/inLab HT A1 I12/5 EUDAMED
Device Name
IPS e.max CAD EUDAMED
Model / Reference
626391 EUDAMED

Identifiers

Primary DI / UDI-DI
07615208367881 EUDAMED
Basic UDI-DI
76152082ACERA001EQ EUDAMED
Unit of Use DI
07615208586770 EUDAMED
EMDN Code
Q010699 MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Liechtenstein EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

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

IPS e.max CAD CEREC/inLab HT A1 I12/5 by Ivoclar Vivadent AG — Class IIa — 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
Ivoclar Vivadent AG
EUDAMED SRN
LI-MF-000000522

Sources (1)

  • EUDAMED 620c1521-20af-425b-920a-7162d33e20fd 61 fields · synced Oct 6, 2026