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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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SIM MICRO CANNULA — 151 UDI-DI variants, MDR

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

Data from EUDAMED, last updated May 31, 2026

SIM MICRO CANNULA

803360952CANNULEG9

151 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

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UDI-DI variants

151 UDI-DI variants

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Applied filters

basicUdiUlid01KAE7WQG7CPRKVZ6XBNCYS4S7

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

PD-DS-201508033609528929
CSSR40G8008033609522460
CSSR30W16008033609523993
CSSR30J16008033609522828
CSSR30V16008033609524006
CSSR40L16008033609522323
CSSR20J16008033609523979
CSSR40I13008033609523047
CSSR30S14008033609521876
CSSR20L16008033609522293
CSSR30S16008033609521777
CSSR20L13008033609522286
CSSR20G8008033609522408
CSSR20F15008033609523092
CSSR40D16008033609522811
CSSR20Y13008033609523900
CSSR40T160S08033609525782
CSSR40S14008033609521883
CSSR14F15008033609524501
CSSR30F15008033609523108
CSSR05X9008033609524037
CSSR30S13008033609521791
CSSR20O13008033609523467
CSSR40S16008033609521784
KIT 006 08033609528486

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803360952CANNULEG9
Device name: SIM MICRO CANNULA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
SRN: IT-MF-000026962
Country: Italy
Email: info@medeurope.eu
Phone: +39 051810572

Variants by status