← Back to catalogue

Polytrap

EUDAMED

Class I (EU MDR)

Ref MIS1-POLYPTRAP

by Poirot Plastique Industrie Médical

Identity

Trade Name
Polytrap EUDAMED
Device Name
1-TRAP EUDAMED
Model / Reference
MIS1-POLYPTRAP EUDAMED

Identifiers

Primary DI / UDI-DI
03760312990525 EUDAMED
Basic UDI-DI
37603129910017130TRAPZ2 EUDAMED
Direct Marketing DI
03760312990525 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

Polytrap 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
FR-MF-000023833

Sources (1)

  • EUDAMED b656c809-caf8-434b-8858-d12ef70694af 61 fields · synced Jun 18, 2026