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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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Plastic spectacle frame for corrective… — 161 UDI-DI variants, MDR

MD Atlas
Stiloptic di Celer Patrycja Ewa

Data from EUDAMED, last updated May 31, 2026

Plastic spectacle frame for corrective lenses

805415467AQ02100202CR

161 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: Stiloptic di Celer Patrycja Ewa

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805415467AQ02100202CR
Device name: Plastic spectacle frame for corrective lenses
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Stiloptic di Celer Patrycja Ewa
SRN: IT-MF-000027197
Country: Italy
Email: info@stiloptic.com
Phone: +39 0323800939

Variants by status

UDI-DI variants

161 UDI-DI variants

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Applied filters

basicUdiUlid01KMJ5NT8R9EAVA0NF9SYBQJYF

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

SI7030.19380541546728998
SI7030.24480541546729360
SI7031.24180541546729742
SI7031.24280541546729810
SI7032.19980541546735132
SI7032.22880541546735200
SI7032.25180541546735378
SI7032.25480541546735446
SI7037.26880541546742758
SI7039.26880541546743366
SI5011.08680541546702608

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