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Explorer Seingle Ended

EUDAMED

Class I (EU MDR)

Ref S-516-23

by Seven Eight Sirgikal

Identity

Trade Name
EXPLORER SEINGLE ENDED EUDAMED
Device Name
DENTAL EXPLORERS EUDAMED
Model / Reference
S-516-23 EUDAMED

Identifiers

Primary DI / UDI-DI
+G276S516230V EUDAMED
Basic UDI-DI
++G276EXPLORERSXF EUDAMED
EMDN Code
L031102 EXPLORATION PROBES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Explorer Seingle Ended by Seven Eight Sirgikal — 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
PK-MF-000009959
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 2b772c21-bb20-41ac-b07b-528dab253e30 61 fields · synced Jul 9, 2026