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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-Guard — 8 UDI-DI variants, MDR (Poirot Plastique Industrie Médical)

MD Atlas
Poirot Plastique Industrie Médical

Data from EUDAMED, last updated May 19, 2026

1-Guard

37603129910018000OBCB

8 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: 37603129910018000OBCB
Device name: 1-Guard
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2025

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

8 UDI-DI variants

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Applied filters

basicUdiUlid01JJ7046DR359GP7CCHZKAKHJD

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

1001801103760312990273
1001800003760312990013
10018000503760312990044
AN236000003760312990310
1-guard plus mini03760312990419
1001800303760312990334
1001800203760312990020
10018000/R03760312990372