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Weldon Instruments

EUDAMED

Class I (EU MDR)

Ref WD-071-088R

by Weldon Instruments

Identity

Trade Name
WELDON INSTRUMENTS EUDAMED
Device Name
WD-071-088R: Non-Sterile, Reusable, Flohr Root Elevator Fig.2 EUDAMED
Model / Reference
WD-071-088R EUDAMED

Identifiers

Primary DI / UDI-DI
05056863316920 EUDAMED
Basic UDI-DI
B-05056863316920 EUDAMED
EMDN Code
L150201 DENTAL RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Weldon Instruments by Weldon Instruments — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Weldon Instruments
EUDAMED SRN
PK-MF-000010180
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 812706ef-ba6e-4c02-8811-8f30319d435d 61 fields · synced May 22, 2026