← Back to catalogue

Nemca135

EUDAMED

Class I (EU MDR)

Ref NEMCA135

by NorthEast Monitoring, Inc.

Identity

Trade Name
NEMCA135 EUDAMED
Device Name
DR200 patient cable EUDAMED
Model / Reference
NEMCA135 EUDAMED

Identifiers

Primary DI / UDI-DI
+M582NEMCA1350 EUDAMED
Basic UDI-DI
++M582NEMCABH EUDAMED
Direct Marketing DI
+M582NEMCA1350 EUDAMED
EMDN Code
Z12030680 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

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

Nemca135 by NorthEast Monitoring, 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

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

Manufacturer

EUDAMED SRN
US-MF-000019819
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 440e4eb6-d874-49bc-9dad-ba0b7bfe0d2e 61 fields · synced Jun 18, 2026