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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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Fiber Light Guides — 211 UDI-DI variants, MDR

MD Atlas
RfQ-Medizintechnik GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Fiber Light Guides

426074483095AT

211 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: RfQ-Medizintechnik GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074483095AT
Device name: Fiber Light Guides
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: RfQ-Medizintechnik GmbH & Co. KG
SRN: DE-MF-000007646
Country: Germany
Email: info@rfq.de
Phone: +49 7461 96170

Variants by status

UDI-DI variants

211 UDI-DI variants

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Applied filters

basicUdiUlid01KKGPKKYKGCPA7BFMNEF0ZGYT

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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00211106804260744830110
00212106904260744830226
00212106104260744830165
00212106004260744830158

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