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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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fullrim plastic spectacle frames — 335 UDI-DI variants, MDR

MD Atlas
Alpha Collection

Data from EUDAMED, last updated May 23, 2026

fullrim plastic spectacle frames

42559085F-PLA-FUL-ADL-3S

335 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: Alpha Collection

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 42559085F-PLA-FUL-ADL-3S
Device name: fullrim plastic spectacle frames
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Alpha Collection
SRN: DE-MF-000050363
Country: Germany
Email: alpha.optics@gmx.net
Phone: +49 30 8322 5031

Variants by status

UDI-DI variants

335 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ30Z3ZD2XM70E6BQS7FTAQB

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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