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HARTMAN FORCEPS 10cm

EUDAMED

Class I (EU MDR)

Ref 17-120 RIRef 17-122 RI

by Raydent Instruments

Identity

Trade Name
HARTMAN FORCEPS 10cm EUDAMED
Device Name
HARTMAN FORCEPS 10cm EUDAMED
Model / Reference
17-120 RI EUDAMED
17-122 RI EUDAMED

Identifiers

Primary DI / UDI-DI
G26817120RI0 EUDAMED
G26817122RI0 EUDAMED
Basic UDI-DI
++G26817120RIXR EUDAMED
++G26817122RIY3 EUDAMED
EMDN Code
L031399 GENERAL SURGERY FORCEPS, REUSABLE - OTHER 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

HARTMAN FORCEPS 10cm 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 a938d173-c10e-4079-a081-a3899fa7058e 61 fields · synced Jul 23, 2026
  • EUDAMED 6feb17c8-5c2f-4039-ab7d-5f82cc14c171 61 fields · synced May 18, 2026