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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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C-Modeler clase I — 16 UDI-DI variants, MDR (DM CEOSA)

MD Atlas
DM CEOSA

Data from EUDAMED, last updated May 23, 2026

C-Modeler clase I

84356459121UM

16 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: DM CEOSA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84356459121UM
Device name: C-Modeler clase I
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: DM CEOSA
SRN: ES-MF-000000579
Country: Spain
Email: aperez@ortoceosa.net
Phone: +34 916441276

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMMNMEGXNB0R95YNB46JTDAS

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

2261-0118435645912675
2261-2118435645912798
2261-0318435645912699
2261-2318435645912811
2261-0218435645912682
2261-2218435645912804
2261-2418435645912828
2261-0418435645912705
2261-1018435645912767
2261-0718435645912736
2261-0618435645912729
2261-1218435645912781
2261-0918435645912750
2261-0518435645912712
2261-1118435645912774
2261-0818435645912743