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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 VISCOFLEX® P161M — 5 UDI-DI variants, MDR

MD Atlas
SYSTEM ASSISTANCE MEDICAL

Data from EUDAMED, last updated May 19, 2026

SYST'AM VISCOFLEX® P161M

37003686P161MOPPHI1HC

5 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: 37003686P161MOPPHI1HC
Device name: SYST'AM VISCOFLEX® P161M
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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KC1X5Q52C02K7HNNPM1DBMC2

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

P161MOPPMHABX03700368628928
P161MOPPMHI03700368611913
P161MOPPMHIBX03700368624128
P161MOPPMHINC03700368611937
P161MOPPMHINCBX03700368624319