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Ergoplant

EUDAMED

Class I (EU MDR)

Ref DX709

by Aesculap AG

Identity

Trade Name
ERGOPLANT EUDAMED
Device Name
Dental instrument set Ir EUDAMED
Model / Reference
DX709 EUDAMED

Identifiers

Primary DI / UDI-DI
04038653457939 EUDAMED
Basic UDI-DI
40392390000018042N EUDAMED
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Ergoplant by Aesculap AG — 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
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED 6d5ba1b6-bc99-4b86-b352-e8feff3faa14 61 fields · synced Jun 19, 2026