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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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LYSETTE ELÁSTICO TS DÍA- 2X20 — 31 UDI-DI variants, MDR

MD Atlas
Activ Medical Disposable

Data from EUDAMED, last updated May 19, 2026

LYSETTE ELÁSTICO TS DÍA- 2X20

3770003083SLIPXK

31 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: Activ Medical Disposable

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770003083SLIPXK
Device name: LYSETTE ELÁSTICO TS DÍA- 2X20
Device model: CHANGE COMPLET
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Activ Medical Disposable
SRN: FR-MF-000009503
Country: France
Email: amdfrance@activmed.eu
Phone: 04.66.80.77.01

Variants by status

UDI-DI variants

31 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JKFXBRYA6AGK1HDKQ3RKWAS5

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

1101300203701116401114
1104320203701116402166
1104310203701116401091
1103300103770003083115
1103400103770003083122
1102301103770003083092

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