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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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Bare Fiber — 85 UDI-DI variants, MDR (CeramOptec GmbH)

MD Atlas
CeramOptec GmbH

Data from EUDAMED, last updated May 23, 2026

Bare Fiber

404905902N2

85 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: CeramOptec GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 404905902N2
Device name: Bare Fiber
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: CeramOptec GmbH
SRN: DE-MF-000005607
Country: Germany
Email: QM@biolitec.com
Phone: +49 228 97 967 0

Variants by status

UDI-DI variants

85 UDI-DI variants

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Applied filters

basicUdiUlid01KBCK5HMZ3YFWTG98ES9BK77H

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

50320192104049059516748
50320074504049059517974
50120101704049059516397
50220073704049059515697
50180574004049059517752
50120031404049059514485
50320080004049059518414
50180529204049059517455
50110046004049059519084
50220075104049059515581

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