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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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Viscorib 1.0 — 2 UDI-DI variants, MDR (IROMED GROUP S.R.L.)

MD Atlas
IROMED GROUP S.R.L.

Data from EUDAMED, last updated May 30, 2026

Viscorib 1.0

805701817S10VA4

2 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: IROMED GROUP S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805701817S10VA4
Device name: Viscorib 1.0
Device model: Viscorib 1.0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: IROMED GROUP S.R.L.
SRN: IT-MF-000031267
Country: Italy
Email: regulatoryaffairs@iromedgroup.com
Phone: +39 06 92595490

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KHZXPGJX8C5TRBYQ9D52B6ZG

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

S10V003V08057018170388
S10V004V08057018170791