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Hi-Line Xs

EUDAMED

Class IIa (EU MDR)

Ref GE644R

by Aesculap AG

Identity

Trade Name
HI-LINE XS EUDAMED
Device Name
PS-Tools rotating instrument sterile RU EUDAMED
Model / Reference
GE644R EUDAMED

Identifiers

Primary DI / UDI-DI
04038653379446 EUDAMED
Basic UDI-DI
403923900000267132 EUDAMED
EMDN Code
Z12100980 INSTRUMENTS FOR MOTORISED NEUROSURGERY SYSTEMS - HARDWARE ACCESSORIES 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

Hi-Line Xs by Aesculap AG — Class IIa — 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 9d3763b5-921e-4ce3-b9b1-0a8dd481d6e0 61 fields · synced May 22, 2026