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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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CeraRoot® Ceramic Transporter — 7 UDI-DI variants, MDR (CeraRoot SL)

MD Atlas
CeraRoot SL

Data from EUDAMED, last updated May 23, 2026

CeraRoot® Ceramic Transporter

84354539CTEG

7 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: CeraRoot SL

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 84354539CTEG
Device name: CeraRoot® Ceramic Transporter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: CeraRoot SL
SRN: ES-MF-000000251
Country: Spain
Email: josep.oliva@ceraroot.com
Phone: +34 937 68 39 62

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GEKV9AQ1WG52NZ7G45V4J3VG

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

006.01108435453900546
006.11108435453901086
006.01208435453900553
006.01608435453900522
006.01708435453900539
006.02108435453900560
006.03408435453900577