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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 Spectacle Frames Without Lenses — 58 UDI-DI variants, MDR

MD Atlas
NOKI Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság

Data from EUDAMED, last updated May 24, 2026

Metal Spectacle Frames Without Lenses

599957378Q02100201WP

58 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: NOKI Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 599957378Q02100201WP
Device name: Metal Spectacle Frames Without Lenses
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: NOKI Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
SRN: HU-MF-000027260
Country: Hungary
Email: nokipisti@t-online.hu

Variants by status

UDI-DI variants

58 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GGPJJ5JYKHPVD57A1F509V59

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

ITTE03605999573780547
ITTE03805999573780554
ITTE03905999573780561
LDT05705999573780530
WRE01205999573780073
WRE01305999573780080
WRE01405999573780097
WRE01505999573780103

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