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Prospace

EUDAMED

Class I (EU MDR)

Ref SJ884R

by Aesculap AG

Identity

Trade Name
PROSPACE EUDAMED
Device Name
PROSPACE/TSPACE dissecting instrument EUDAMED
Model / Reference
SJ884R EUDAMED

Identifiers

Primary DI / UDI-DI
04046963955205 EUDAMED
Basic UDI-DI
4039239000000431ZT EUDAMED
Direct Marketing DI
04046963955205 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS 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

Prospace 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 24bc26c1-48ca-48e3-84b3-ff4e92761511 61 fields · synced May 22, 2026