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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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Tubo para cementado directo — 64 UDI-DI variants, MDR (DM CEOSA)

MD Atlas
DM CEOSA

Data from EUDAMED, last updated May 23, 2026

Tubo para cementado directo

84356459214BJM

64 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: 84356459214BJM
Device name: Tubo para cementado directo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 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

64 UDI-DI variants

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Applied filters

basicUdiUlid01KJ7VAZG7P1N4VSZHK2RR2CZY

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

No registered UDI-DI variants for this device family.