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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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RIUNITI OFTALMICI — 4 UDI-DI variants, MDR (Nelthema srls)

MD Atlas
Nelthema srls

Data from EUDAMED, last updated May 31, 2026

RIUNITI OFTALMICI

805662865FAM0018R

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Nelthema srls

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805662865FAM0018R
Device name: RIUNITI OFTALMICI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nelthema srls
SRN: IT-MF-000051529
Country: Italy
Email: n.sonnino@nelthema-group.com
Phone: +393459459298

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KH1JB6E1ZM309KTYJP8SFFBM

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

Excellence II08056628650037
65SA.N08056628650020
New Simplex III08056628650013
Newline II08056628650006