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Ecor

EUDAMED

Class IIa (EU MDR)

Ref 12016-08003Model gammaCore Sapphire SLC Evaluation Kit 93-Day ( Kit with refill card)

by ElectroCore, Inc.

Identity

Trade Name
ECOR EUDAMED
Device Name
gammaCore Sapphire SLC EUDAMED
Model / Reference
gammaCore Sapphire SLC Evaluation Kit 93-Day ( Kit with refill card) EUDAMED
12016-08003 EUDAMED

Identifiers

Primary DI / UDI-DI
00815203021192 EUDAMED
Basic UDI-DI
B-00815203021192 EUDAMED
EMDN Code
Z12101106 NEUROLOGICAL STIMULATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Point aesthesiometer

Ecor by ElectroCore, Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Point aesthesiometer.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
ElectroCore, Inc.
EUDAMED SRN
US-MF-000036987
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 38ac7611-c1f1-489b-8cf1-80f004a68941 61 fields · synced Jun 19, 2026