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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 P501P — 15 UDI-DI variants, MDR (SYSTEM ASSISTANCE MEDICAL)

MD Atlas
SYSTEM ASSISTANCE MEDICAL

Data from EUDAMED, last updated May 19, 2026

SYST'AM P501P

37003686P501PAHW1DN

15 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: 37003686P501PAHW1DN
Device name: SYST'AM P501P
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 29, 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

15 UDI-DI variants

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Applied filters

basicUdiUlid01KDNFT75Y7E46687DJKTYGKZM

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

P501PA2824W03700368601167
P501PA3636W03700368614198
P501PA4040W03700368614211
P501PA4043W03700368614235
P501PA4046W03700368614259
P501PA4343W03700368614273
P501PA4346W03700368628812
P501PA4640W03700368614297
P501PA4646W03700368614310
P501PA5146W03700368614334
P501PA5150W03700368614358
P501PA5646W03700368628829
P501PA6150W03700368628836
P501PAB4040W03700368624456
P501PAB4343W03700368624463