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Ennovate®

EUDAMED

Class IIb (EU MDR)

Ref SY990KS

by Aesculap AG

Identity

Trade Name
Ennovate® EUDAMED
Device Name
ENNOVATE implant, sterile EUDAMED
Model / Reference
SY990KS EUDAMED

Identifiers

Primary DI / UDI-DI
04046955204991 EUDAMED
Basic UDI-DI
40392390000012962P EUDAMED
EMDN Code
P09070304 SPINE FIXATION SYSTEM CONNECTORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

Yes

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

Ennovate® by Aesculap AG — Class IIb — 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 faba242a-00d9-4058-9e78-fce8a0f1de64 61 fields · synced Jun 19, 2026