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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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Fiberoptic cable — 2 UDI-DI variants, MDR (Erbe Vision GmbH)

MD Atlas
Erbe Vision GmbH

Data from EUDAMED, last updated May 23, 2026

Fiberoptic cable

426021465FOCC3

2 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: Erbe Vision GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 426021465FOCC3
Device name: Fiberoptic cable
Device model: Fiberoptic cable
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Erbe Vision GmbH
SRN: DE-MF-000010268
Country: Germany
Email: prrc@erbe-vision.com
Phone: +49 7461 908460

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HYWFENZHKNEQ0RNJ9EAQYRQN

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

Fiberoptic cable Ø 4.8 mm; L 3m04260214650323
Fiberoptic cable, Ø 3.5 mm; L 3m04260386576315