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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 — 5 UDI-DI variants, MDR (EUROBASTON, S.L. - NIF B33851155)

MD Atlas
EUROBASTON, S.L. - NIF B33851155

Data from EUDAMED, last updated May 30, 2026

BASTON

843702316801CG

5 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: EUROBASTON, S.L. - NIF B33851155

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843702316801CG
Device name: BASTON
Device model: 0100,01030,1005,01070,01090
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: EUROBASTON, S.L. - NIF B33851155
SRN: ES-MF-000025336
Country: Spain
Email: INFO@EUROBASTON.COM
Phone: +34 9 8532 13 95

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KSASCME3P6FM1ASTC9K3F8H3

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

0109008437023168035
0107008437023168028
0105008437023168011
0103008437023168004
010108437023168042