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Ennovate®

EUDAMED

Class IIa (EU MDR)

Ref SZ137SU

by Aesculap AG

Identity

Trade Name
Ennovate® EUDAMED
Device Name
ENNOVATE C instrument IIa SU sterile EUDAMED
Model / Reference
SZ137SU EUDAMED

Identifiers

Primary DI / UDI-DI
04046955181285 EUDAMED
Basic UDI-DI
40392390000026252T EUDAMED
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Joint prosthesis implantation kit, single-use

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

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

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 6ae60358-f76c-4445-aa07-504fbaf4519e 61 fields · synced Jun 19, 2026