Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

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

50520092004049059519022
50330040504049059516977
50320029004049059518759
50330041504049059518193
50320074104049059516946
50220088504049059515451
50320191904049059517035
50310045004049059518766
50350050004049059518117
50020032604049059515871
50320050504049059517899
50320074004049059516885
50120075004049059515963
50130040004049059514706
50130041504049059516496
50320074404049059517530
50120074804049059516472
50320012004049059519336
50320015004049059519367
50320011004049059519312
50320031504049059516922
50120074204049059514546
50020032804049059515086
50130040504049059514713
50350053004049059518100

1 2 3 4