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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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Bracket de autoligado — 168 UDI-DI variants, MDR (DM CEOSA)

MD Atlas
DM CEOSA

Data from EUDAMED, last updated May 23, 2026

Bracket de autoligado

84356459231UV

168 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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UDI-DI variants

168 UDI-DI variants

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Applied filters

basicUdiUlid01KJQAJDMXP5139M86DBZTZGEY

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

1292-42AS-1ºDAK18435645906117
1292-43BS-11ºEFG18435645906223
1292-43AS-11ºEFG18435645906209
1292-44BS-14ºDAG18435645906315
1292-44AS-14ºDAG18435645906261
1292-45BS-17ºDAG18435645906384
1292-45AS-17ºDAG18435645906346
1292-45AS-17ºDEG18435645906353
1292-46AS+25ºFAI18435645906391
1292-5318435645906452
1292-5018435645906421
1292-11BS+16ºEFG18435645904908
1292-12BS+10ºDIK18435645904991
1292-13BS+0ºEKE18435645905080
1292-14BS-7ºDAE18435645905158
1292-15BS-7ºDAE18435645905219
1292-21BS+16ºEFG18435645905301
1292-22BS+10ºDJK18435645905387
1292-23BS+0ºEKE18435645905479
1292-24BS-7ºDAE18435645905547
1292-25BS-7ºDAE18435645905608
1292-31BS-2ºDAK18435645905707
1292-32BS-2ºDAK18435645905776
1292-33BS-4ºEFG18435645905851
1292-34BS-11ºDAG18435645905929

3 4 5 6 7

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84356459231UV
Device name: Bracket de autoligado
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