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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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TONICROSS PLUS — 4 UDI-DI variants, MDR (RUPIANI)

MD Atlas
RUPIANI

Data from EUDAMED, last updated May 19, 2026

TONICROSS PLUS

376032952TPLUS01994

4 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: RUPIANI

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376032952TPLUS01994
Device name: TONICROSS PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 30, 2023

Manufacturer & authorised representative

Manufacturer

Name: RUPIANI
SRN: FR-MF-000001715
Country: France
Email: affairesreglementaires@rupiani.fr

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HBKVMQBHRR9J5K4JKN3K5AF9

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

TONICROSS PLUS03760329520081
TONICROSS PLUS03760329520067
TONICROSS PLUS03760329520074
TONICROSS PLUS03760329520098