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Columbia Cheek Retractor Double Ended

EUDAMED

Class I (EU MDR)

Ref PI005

by Promed Instruments

Identity

Trade Name
Columbia Cheek Retractor Double Ended EUDAMED
Device Name
Columbia Cheek Retractor Double Ended EUDAMED
Model / Reference
PI005 EUDAMED

Identifiers

Primary DI / UDI-DI
G796PI0050 EUDAMED
Basic UDI-DI
++G796PI0055C EUDAMED
EMDN Code
L150201 DENTAL RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Columbia Cheek Retractor Double Ended by Promed Instruments — 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
Promed Instruments
EUDAMED SRN
PK-MF-000049405
Authorised Representative
International Business Compendious of Sweden SE-AR-000001625

Sources (1)

  • EUDAMED 6963b79c-60a8-4531-8eec-8b10444888df 61 fields · synced Jun 19, 2026