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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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Arco facial Standard — 32 UDI-DI variants, MDR (DM CEOSA)

MD Atlas
DM CEOSA

Data from EUDAMED, last updated May 23, 2026

Arco facial Standard

84356459112UL

32 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: 84356459112UL
Device name: Arco facial Standard
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 24, 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

32 UDI-DI variants

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Applied filters

basicUdiUlid01KMFZN3PFK4TPAQQSAW04RSJE

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

2254-1518435645912651
2254-0418435645912552
2254-0818435645912590
2254-0918435645912606
2254-1018435645912613
2254-1618435645912668
2254-1218435645912637

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