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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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ANIOS LB 300 4X5L — 2 UDI-DI variants, MDR (Laboratoires Anios)

MD Atlas
Laboratoires Anios

Data from EUDAMED, last updated May 19, 2026

ANIOS LB 300 4X5L

359761LA0150DNLIRZ

2 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: Laboratoires Anios

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 359761LA0150DNLIRZ
Device name: ANIOS LB 300 4X5L
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2025

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

2 UDI-DI variants

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Applied filters

basicUdiUlid01JV9BEAWR5D585D929T1Q9KGA

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

2160034ZI03597610647055
2161038ZI03597610647079