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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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Ligadura elástica — 14 UDI-DI variants, MDR (DM CEOSA)

MD Atlas
DM CEOSA

Data from EUDAMED, last updated May 23, 2026

Ligadura elástica

84356459222UU

14 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: DM CEOSA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84356459222UU
Device name: Ligadura elástica
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 2, 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

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJPYJGY0VC388QAYSP9EACH8

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

2121-0618435645910701
2121-0818435645910725
2121-0918435645910732
2121-1118435645910756
2121-1318435645910770
2121-4418435645910800
2121-2118435645910794
2121-1218435645910763
2121-1018435645910749
2121-0518435645910695
2121-1418435645910787
2121-0118435645910671
2121-0318435645910688
2121-0718435645910718