Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

SI5027.30780541546756090
SI5027.30880541546756168
SI5027.31280541546756236
SI5028.30780541546756304
SI5028.30880541546756472
SI5028.30980541546756540
SI5028.31380541546756618
SI5032.28180541546758698
SI5032.30180541546758766
SI5032.31280541546758834
SI5032.32380541546758902
SI5032.32480541546759060
SI5033.28980541546762626
SI5033.30480541546762794
SI5033.33680541546762312
SI5033.33780541546762480
SI5033.33880541546762558
SI5033.34080541546762862
SI5034.27780541546763098
SI5034.31280541546762930
SI5034.32580541546763234
SI5034.32680541546763166
SI5034.33980541546763302
SI5036.27780541546765528
SI5036.34180541546765696

1 2 3 4 5