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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 VARISPORT — 7 UDI-DI variants, MDR

MD Atlas
Fleming Comercial, S.A.

Data from EUDAMED, last updated May 23, 2026

TOBILLERA VARISPORT

8426828tobilleraNB

7 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: Fleming Comercial, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8426828tobilleraNB
Device name: TOBILLERA VARISPORT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: Fleming Comercial, S.A.
SRN: ES-MF-000004259
Country: Spain
Email: fleming-sa@fleming-sa.com
Phone: +34934902946

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G9F3058P892G1ZYT17FVV6Y4

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

234203408426828420349
234203508426828420356
234203608426828420363
234203008426828420301
234203108426828420318
234203208426828420325
234203308426828420332