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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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Optima — 60 UDI-DI variants, MDR (OPTIMA MOLLITER SRL)

MD Atlas
OPTIMA MOLLITER SRL

Data from EUDAMED, last updated May 30, 2026

Optima

805715830OPTIMALZ

60 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: OPTIMA MOLLITER SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805715830OPTIMALZ
Device name: Optima
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 11, 2022

Manufacturer & authorised representative

Manufacturer

Name: OPTIMA MOLLITER SRL
SRN: IT-MF-000022195
Country: Italy
Email: info@optimamolliter.com
Phone: +390733801060

Variants by status

UDI-DI variants

60 UDI-DI variants

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Applied filters

basicUdiUlid01GHJX9HTKHQ56G04M2QKRATWF

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

TO-LIGHTS08054794757413
TO-POST001XL08057158300133
PLO-CL001M08057158302533
TO-EUR001XL08057158300188
TO-CLH001S08057158300058
PLO-OPKIT001M08057158301024
TO-GROUNDM08054794757376
TO-LGHT01M08054794782101
PLO-OPKIT001XXL08057158301055
TO-EUR001L08057158300171

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