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Parathyroid Imaging System

EUDAMED

Class I (EU MDR)

Ref ARGOS-200PT

by Shinevia (Shandong) Technology Co., Ltd.

Identity

Trade Name
Parathyroid Imaging System EUDAMED
Device Name
Parathyroid Imaging System EUDAMED
Model / Reference
ARGOS-200PT EUDAMED

Identifiers

Primary DI / UDI-DI
16976982090807 EUDAMED
Basic UDI-DI
697698209PIS2C EUDAMED
Direct Marketing DI
16976982090807 EUDAMED
EMDN Code
Z11069080 VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Parathyroid Imaging System by Shinevia (Shandong) Technology Co., Ltd. — 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
CN-MF-000049465
Authorised Representative
Everbiz GmbH DE-AR-000008964

Sources (1)

  • EUDAMED d03f0e1b-cf57-4c9f-a046-c74442a96f87 61 fields · synced Jul 9, 2026