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Beckmann Curette

EUDAMED

Class I (EU MDR)

Ref 41-525 RIRef 41-520 RI

by Raydent Instruments

Identity

Trade Name
BECKMANN CURETTE EUDAMED
Device Name
BECKMANN CURETTE EUDAMED
Model / Reference
41-525 RI EUDAMED
41-520 RI EUDAMED

Identifiers

Primary DI / UDI-DI
G26841525RI0 EUDAMED
G26841520RI0 EUDAMED
Basic UDI-DI
++G26841525RIZ3 EUDAMED
++G26841520RIYA EUDAMED
EMDN Code
L149001 ENT CURETTES, 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

Beckmann Curette by Raydent 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
Raydent Instruments
EUDAMED SRN
PK-MF-000032781
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (2)

  • EUDAMED 172fa30a-bf4f-44f8-843b-51c25a3db1df 61 fields · synced Jul 15, 2026
  • EUDAMED 718748a7-73c5-40ef-950d-276e063198db 61 fields · synced May 18, 2026