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Poole 30fg

EUDAMED

Class I (EU MDR)

Ref 5-240 RI

by Raydent Instruments

Identity

Trade Name
POOLE 30FG EUDAMED
Device Name
POOLE 30FG EUDAMED
Model / Reference
5-240 RI EUDAMED

Identifiers

Primary DI / UDI-DI
G2685240RI0 EUDAMED
Basic UDI-DI
++G2685240RID4 EUDAMED
EMDN Code
L030101 SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, 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

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Poole 30fg by Raydent Instruments — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.

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 (1)

  • EUDAMED c1a4255d-9ff7-4d9c-aa84-223fadf5a7ae 61 fields · synced Jun 19, 2026