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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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Accessories - Test Strip — 32 UDI-DI variants, MDR

MD Atlas
Laboratoires Anios

Data from EUDAMED, last updated May 19, 2026

Accessories - Test Strip

359761LA01571BTSPY

32 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: 359761LA01571BTSPY
Device name: Accessories - Test Strip
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

32 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KE9PQ0HJSCR229PQVHFRQW5M

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

100110EK03597610460135
100987YL03597610663604
100987FH03597610672330
10098703597610003943
100987PL03597610572296
100987E103597610516832
100987AV03597610600791

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