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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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ARTOX 2% (1 siringa preriempita) — 12 UDI-DI variants, MDR

MD Atlas
GRUPPO FARMAIMPRESA SRL

Data from EUDAMED, last updated May 30, 2026

ARTOX 2% (1 siringa preriempita)

805574884FTMDR74YE

12 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: GRUPPO FARMAIMPRESA SRL

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Device characteristics

Implantable

Legacy certificates

Certificate number: 009-00-19-MDR
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ITALCERT SRL (0426)
Validity: May 19, 2026 → Jan 9, 2028

Certificate number: 020-00-04-MDR
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ITALCERT SRL (0426)
Validity: Jun 9, 2025 → Jun 21, 2028

Certificate number: 021-00-05-MDR
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ITALCERT SRL (0426)
Validity: May 19, 2026 → Jun 21, 2028

Identity & classification

Basic UDI-DI: 805574884FTMDR74YE
Device name: ARTOX 2% (1 siringa preriempita)
Device model: Acido ialuronico sale sodico 2% per iniezione intra-articolare
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Aug 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: GRUPPO FARMAIMPRESA SRL
SRN: IT-MF-000012625
Country: Italy
Email: info@farmaimpresa.it

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H8KTNK9CYP3Q8B6C3FPJE7J8

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

Artox 1.6% (1 prefilled syringe)08055748843510
Artox 1.6% (3 prefilled syringes)08055748843527
Artox 2% (1 prefilled syringe)08055748840779
Artox 2% (3 prefilled syringes)08055748841042
Ilatrox 2% (1 prefilled syringe)08055748841431
Ilatrox 2% (3 prefilled syringes)08055748843640
Introx 2% (1 prefilled syringe)08055748843671
Introx 2% (3 prefilled syringes)08055748843688
Jesitrox 2% (1 prefilled syringe)08055748843657
Jesitrox 2% (3 prefilled syringes)08055748843664
Leovisc 2% (1 prefilled syringe)08055748843756
FT.MDR.74.27.308055748845217