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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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1-TRAP — 4 UDI-DI variants, MDR (Poirot Plastique Industrie Médical)

MD Atlas
Poirot Plastique Industrie Médical

Data from EUDAMED, last updated May 19, 2026

1-TRAP

37603129910017130TRAPZ2

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Poirot Plastique Industrie Médical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37603129910017130TRAPZ2
Device name: 1-TRAP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 21, 2024

Manufacturer & authorised representative

Manufacturer

Name: Poirot Plastique Industrie Médical
SRN: FR-MF-000023833
Country: France
Email: christophe.poirot.ppi@gmail.com
Phone: 0329576819

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JAQMMHCKT9ZT8266FAAFFDE3

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

10017130/R03760312990396
MIS1-POLYPTRAP5003760312990501
MIS1-POLYPTRAP03760312990525
1001713003760312990242