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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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BASTON ERGO BLANDO ALUMINIO — 9 UDI-DI variants, MDR

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

BASTON ERGO BLANDO ALUMINIO

843118411500015CJ

9 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: Ortoiberica S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843118411500015CJ
Device name: BASTON ERGO BLANDO ALUMINIO
Device model: K-11500-015
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ortoiberica S.L.
SRN: ES-MF-000025780
Country: Spain
Email: welcome@ortoiberica.es
Phone: +34985794800

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01GZZSX9BDJ1AEGPC5NSFSQ2JE

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

K-11517-01508431184517008
K-11518-01508431184518005
K-11500-01508431184115006
K-11516-01508431184516018
K-11510-01508431184510009
K-11520-01508431184520008
K-11514-01508431184514014
K-11519-01508431184519002
K-11513-01508431184513017