← Back to catalogue

Oringer Retractor

EUDAMED

Class I (EU MDR)

Ref 1008-10BRef 1008-10CRef 1008-10

by Dental Expert

Identity

Trade Name
ORINGER RETRACTOR EUDAMED
Device Name
ORINGER RETRACTOR EUDAMED
Model / Reference
1008-10B EUDAMED
1008-10C EUDAMED
1008-10 EUDAMED

Identifiers

Primary DI / UDI-DI
D123100810B0 EUDAMED
D123100810C0 EUDAMED
D1231008100 EUDAMED
Basic UDI-DI
++D123100810BGU EUDAMED
++D123100810CGW EUDAMED
++D123100810W4 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

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

Oringer Retractor by Dental Expert — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dental Expert
EUDAMED SRN
PK-MF-000024595
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (3)

  • EUDAMED 8b7dd31c-0267-41c1-8f61-ea357a3d47bc 61 fields · synced Jul 22, 2026
  • EUDAMED 49d1e40c-8eb9-4c33-8bf4-faedad33fd96 61 fields · synced May 17, 2026
  • EUDAMED cfd380f8-cc9d-4f0c-be85-fe3c52db5333 61 fields · synced May 18, 2026