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1-Trap

EUDAMED

Class I (EU MDR)

Ref 10017130Ref 10017130/R

by Poirot Plastique Industrie Médical

Identity

Trade Name
1-Trap EUDAMED
Device Name
1-TRAP EUDAMED
Model / Reference
10017130 EUDAMED
10017130/R EUDAMED

Identifiers

Primary DI / UDI-DI
03760312990242 EUDAMED
03760312990396 EUDAMED
Basic UDI-DI
37603129910017130TRAPZ2 EUDAMED
Direct Marketing DI
03760312990242 EUDAMED
EMDN Code
G0305010201 DIGESTIVE ENDOSCOPY, RETRIEVAL BASKET DEVICES, REVOLVING EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

1-Trap by Poirot Plastique Industrie Médical — 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

EUDAMED SRN
FR-MF-000023833

Sources (2)

  • EUDAMED a39092a3-e3cd-49c7-9143-f7ae8a3dbdfe 61 fields · synced Oct 6, 2026
  • EUDAMED 27fe8df1-fdd7-443f-bab7-956eac80ea47 61 fields · synced May 18, 2026