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Orringer Retractor Large

EUDAMED

Class I (EU MDR)

Ref MD5503

by Medspo

Identity

Trade Name
Orringer Retractor Large EUDAMED
Device Name
Orringer Retractor Large EUDAMED
Model / Reference
MD5503 EUDAMED

Identifiers

Primary DI / UDI-DI
G520MD55030 EUDAMED
Basic UDI-DI
++G520MD5503LE EUDAMED
EMDN Code
L150201 DENTAL RETRACTORS, 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

Orringer Retractor Large 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 b47ba914-d573-461d-b195-e4947eb247c2 61 fields · synced Jul 19, 2026