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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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Desinfectant - T&NT - I&NI — 6 UDI-DI variants, MDR

MD Atlas
Laboratoires Anios

Data from EUDAMED, last updated May 19, 2026

Desinfectant - T&NT - I&NI

359761LA2A452TWI2T

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Laboratoires Anios

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 359761LA2A452TWI2T
Device name: Desinfectant - T&NT - I&NI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Laboratoires Anios
SRN: FR-MF-000011756
Country: France
Email: contact@anios.com
Phone: +33 3 20 67 67 67

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KE9NWDSQWD4E5QJ3JJ2G09F8

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

311413004028163114132
311411004028163114118
311423004028163114149
313819103597610663567
311415004028163114163
315104703597610671180