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 (Ceram Optec SIA)

MD Atlas
Ceram Optec SIA

Data from EUDAMED, last updated May 30, 2026

Bare Fiber

404908902NP

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: Ceram Optec SIA

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: 404908902NP
Device name: Bare Fiber
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ceram Optec SIA
SRN: LV-MF-000021846
Country: Latvia
Email: infolv@ceramoptec.com
Phone: +371 653 43 646

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

basicUdiUlid01KS4R4Z3SQ4X9TN6RGN9WEG3E

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

50120074204049089003904
50320039104049089005748
50350052004049089004345
50180540004049089004048
50320075004049089004215
50120031404049089004536
50120074404049089003911
50120074004049089003881
50320010504049089005830
50350050104049089004307
50120074604049089003942
50320016504049089005922
50320029004049089004147
50220096104049089004116
50180574004049089004055
50320191904049089004598
50320075504049089004222
50320192104049089004604
50320080004049089004628
50320012004049089005861
50120074504049089003928
50380536004049089004369
501200745-104049089003935
50110046004049089004437
50220073704049089004079

1 2 3 4