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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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SODIUM HYALURONATE 2.4% and SODIUM… — 9 UDI-DI variants, MDR

MD Atlas
IBSA FARMACEUTICI ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

SODIUM HYALURONATE 2.4% and SODIUM CHONDROITIN 1.6% - VISCO-SUPPLETIVE JOINT DEVICE

803363895IA0024T

9 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: IBSA FARMACEUTICI ITALIA SRL

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Device characteristics

Implantable

Clinical investigations

Registered: No

Registered: No

Legacy certificates

Certificate number: EPT 0477.MDR.22/4844
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: Mar 11, 2025 → Jun 6, 2027

Certificate number: EPT 0477.MDR.22/4843
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: Mar 11, 2025 → Jun 6, 2027

Identity & classification

Basic UDI-DI: 803363895IA0024T
Device name: SODIUM HYALURONATE 2.4% and SODIUM CHONDROITIN 1.6% - VISCO-SUPPLETIVE JOINT DEVICE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Dec 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: IBSA FARMACEUTICI ITALIA SRL
SRN: IT-MF-000008111
Country: Italy
Email: info@ibsa.it
Phone: +3903716171

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBFR3KKD03NBB3X5YH3JXQ4A

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

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805368986016008053689860160
805368986018408053689860184
805368986015308053689860153
803363895602108033638956021
805368986014608053689860146
805368986013908053689860139
805368986017708053689860177