Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

UDI-DI variants

151 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

CSSR14X7008033609520466
CSSR30G8008033609522439
CSSR40L13008033609522330
CSSR30S8008033609522033
CSSR40J16008033609524358
KIT 007 08033609528493
CSSR30I13008033609523030
CSSR30L13008033609522309
CSSR40D13008033609522804
CSSR30L16008033609522316
KIT G0808033609525959
CSSR30Z33008033609522712
CSSR40Y13008033609524051
CSSR40Y16008033609525034
KIT G1708033609525867
CSSR30D13008033609522781
KIT G0308033609526000
CSSR20X130S08033609523306
33507008033609526031
CSSR20X80S08033609520855
CSSR30X16008033609520527
CSSR14G9008033609522385
KIT G0908033609525942
CSSR07X9008033609520435
CSSR30B13008033609523542

1 2 3 4 5