← Back to catalogue

Ennovate®

EUDAMED

Class IIb (EU MDR)

Ref SY513TS

by Aesculap AG

Identity

Trade Name
Ennovate® EUDAMED
Device Name
ENNOVATE implant, sterile EUDAMED
Model / Reference
SY513TS EUDAMED

Identifiers

Primary DI / UDI-DI
04046964987892 EUDAMED
Basic UDI-DI
40392390000012962P EUDAMED
EMDN Code
P09070302 THORACOLUMBOSACRAL FIXATION SYSTEMS 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

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: Spinal bone screw, non-bioabsorbable

Ennovate® by Aesculap AG — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED 46507d87-3eac-409b-9efb-decf992a7ab1 61 fields · synced Jun 19, 2026