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Percy Retractor

EUDAMED

Class I (EU MDR)

Ref 29-510 RI

by Raydent Instruments

Identity

Trade Name
PERCY RETRACTOR EUDAMED
Device Name
PERCY RETRACTOR EUDAMED
Model / Reference
29-510 RI EUDAMED

Identifiers

Primary DI / UDI-DI
++G26829510RI2C EUDAMED
Basic UDI-DI
B-++G26829510RI2C EUDAMED
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, 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

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

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

Sources (1)

  • EUDAMED cb624f6a-9eba-4dc2-9c4e-4f58a59c4b75 61 fields · synced Jul 13, 2026