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MR Patient Drape (IMRIS)

EUDAMED

Class I (EU MDR)

Ref NGS-PD-05-E

by ClearPoint Neuro, Inc.

Identity

Trade Name
MR Patient Drape (IMRIS) EUDAMED
Device Name
MR Drape EUDAMED
Model / Reference
NGS-PD-05-E EUDAMED

Identifiers

Primary DI / UDI-DI
00850376007833 EUDAMED
Basic UDI-DI
0850376007808E EUDAMED
EMDN Code
Z12100685 STEREOTACTIC NEUROSURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I 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

MR Patient Drape (IMRIS) by Clearpoint Neuro, Inc. — 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

EUDAMED SRN
US-MF-000010239
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 568b2aba-adbd-4356-a6b7-b500f0be910b 61 fields · synced Jun 19, 2026