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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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SYST'AM P361CA — 34 UDI-DI variants, MDR (SYSTEM ASSISTANCE MEDICAL)

MD Atlas
SYSTEM ASSISTANCE MEDICAL

Data from EUDAMED, last updated May 19, 2026

SYST'AM P361CA

37003686P361CAHW1B7

34 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: SYSTEM ASSISTANCE MEDICAL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37003686P361CAHW1B7
Device name: SYST'AM P361CA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: SYSTEM ASSISTANCE MEDICAL
SRN: FR-MF-000003517
Country: France
Email: systam@systam.com
Phone: 0553405035

Variants by status

UDI-DI variants

34 UDI-DI variants

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Applied filters

basicUdiUlid01KC13ZQ38V95J9VYQDK29XE84

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

P361CA51462HW03700368613641
P361CA51501HW03700368613665
P361CA51502HW03700368613672
P361CA56461HW03700368620168
P361CA56462HW03700368620175
P361CA61501HW03700368620182
P361CA61502HW03700368620199
P361CAPU45461HW03700368613689
P361CAU45461HW03700368613696

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