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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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Silicone Hydrogel lathed contact lens — 32 UDI-DI variants, MDR

MD Atlas
mark'ennovy Personalized Care S.L.

Data from EUDAMED, last updated May 23, 2026

Silicone Hydrogel lathed contact lens

8433108TF02-SiliconeLMN

32 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: mark'ennovy Personalized Care S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8433108TF02-SiliconeLMN
Device name: Silicone Hydrogel lathed contact lens
Device model: Silicone Hydrogel lathed contact lens
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.made-to-order
Version date: Apr 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: mark'ennovy Personalized Care S.L.
SRN: ES-MF-000001436
Country: Spain
Email: QARAMadrid@markennovy.com
Phone: +34 646 16 00 94

Variants by status

UDI-DI variants

32 UDI-DI variants

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Applied filters

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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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