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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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Plancha — 42 UDI-DI variants, MDR (DM CEOSA)

MD Atlas
DM CEOSA

Data from EUDAMED, last updated May 23, 2026

Plancha

84356459122UP

42 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: 84356459122UP
Device name: Plancha
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

42 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMMW0M47NEM9KY6B212VH79Z

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

4499-3718435645913610
4499-5618435645914549
4499-4018435645913672
4499-5918435645914907
4499-4118435645913696
4499-5218435645913818
4499-5418435645914525
4499-5318435645913764
4499-5518435645914532
4499-6018435645914792
4499-6118435645914808
4499-7018435645914877
4499-6218435645914815
4499-7118435645914884
4499-6318435645914822
4499-6418435645914839
4499-6518435645914846

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