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Pt1 & Pt2

EUDAMED

Class I (EU MDR)

Ref MD3303

by Medspo

Identity

Trade Name
PT1 & PT2 EUDAMED
Device Name
PT1 & PT2 EUDAMED
Model / Reference
MD3303 EUDAMED

Identifiers

Primary DI / UDI-DI
G520MD33030 EUDAMED
Basic UDI-DI
++G520MD3303KN EUDAMED
EMDN Code
L159003 DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Pt1 & Pt2 by Medspo — 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

Manufacturer
Medspo
EUDAMED SRN
PK-MF-000037594
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 9bee4c1c-3af1-4a51-851b-bf27cba5d7df 61 fields · synced Jul 21, 2026