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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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Tornillo definitivo para implante — 36 UDI-DI variants, MDR

MD Atlas
Luckler Medical S.L.

Data from EUDAMED, last updated May 23, 2026

Tornillo definitivo para implante

8437025437TORNILLOS_IIbYN

36 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Luckler Medical S.L.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 8437025437TORNILLOS_IIbYN
Device name: Tornillo definitivo para implante
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Luckler Medical S.L.
SRN: ES-MF-000028424
Country: Spain
Email: info@luckler.es
Phone: + 34 985 303 882

Variants by status

UDI-DI variants

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCGM6P6BT3Z3PBYA8Z480AQ9

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

TO-00208437025437313
TO-052A08437025437153
TO-034A08437025437344
TO-025A08437025437078
TO-03808437025437047
TO-011A08437025437375
TO-011BC08437025437368
TO-034C08437025437016
TO-087A08437025437092
TO-035A08437025437245
TO-019F08437025437276

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