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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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TOBILLERA TALLA P-M-G — 3 UDI-DI variants, MDR (VENTUBEL, S.A.)

MD Atlas
VENTUBEL, S.A.

Data from EUDAMED, last updated May 31, 2026

TOBILLERA TALLA P-M-G

8430487TOBILLERATL

3 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: VENTUBEL, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8430487TOBILLERATL
Device name: TOBILLERA TALLA P-M-G
Device model: TOBILLERA TALLA P-M-G
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: VENTUBEL, S.A.
SRN: ES-MF-000039014
Country: Spain
Email: sduran@ventubel.com
Phone: +34916124401

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSNSX386NY7JB7668KWWYV7Y

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 G08430487000187
TO M08470004426083
TO P08470004425901