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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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CINTURON DE SILLA — 6 UDI-DI variants, MDR

MD Atlas
EUROBASTON, S.L. - NIF B33851155

Data from EUDAMED, last updated May 23, 2026

CINTURON DE SILLA

843702316806CS

6 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: 843702316806CS
Device name: CINTURON DE SILLA
Device model: TRONCO
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01KSASWK79FVEZ6XD8VQA3JNV9

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

210308437023168189
0212008437023168196
0210008437023168158
0210108437023168165
210208437023168172
0213008437023168202