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Cheek Retractors

EUDAMED

Class I (EU MDR)

Ref A8-UNO (DRE130)

by Larident SRL

Identity

Trade Name
CHEEK RETRACTORS EUDAMED
Device Name
Apribocca in plastica sterilizzabile EUDAMED
Model / Reference
A8-UNO (DRE130) EUDAMED

Identifiers

Primary DI / UDI-DI
08050503882032 EUDAMED
Basic UDI-DI
8053504980ADEE EUDAMED
Direct Marketing DI
08050503882032 EUDAMED
EMDN Code
L150201 DENTAL RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Cheek Retractors by Larident SRL — 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
Larident SRL
EUDAMED SRN
IT-MF-000007807

Sources (1)

  • EUDAMED 2818b647-713c-404b-b965-b8fb83a56364 61 fields · synced Jun 19, 2026