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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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Metal & Acetate spectacle frame for… — 10 UDI-DI variants, MDR

MD Atlas
Stiloptic di Celer Patrycja Ewa

Data from EUDAMED, last updated May 31, 2026

Metal & Acetate spectacle frame for corrective lenses

805415467AQ02100203CT

10 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: 805415467AQ02100203CT
Device name: Metal & Acetate 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KQYWNXZWR0Z5DN20Y17FX0B6

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

SI6010.56380541546757776
SI6010.65880541546757844
SI6010.65980541546757912
SI6011.56680541546764910
SI6011.64880541546765078
SI6011.65480541546765146
SI6011.65580541546758452
SI6011.66180541546765214
SI6011.66280541546765382
SI6011.66380541546765450