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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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Sujeción para pacientes en quirófano — 4 UDI-DI variants, MDR

MD Atlas
Medi Care System S.L.U.

Data from EUDAMED, last updated May 23, 2026

Sujeción para pacientes en quirófano

843603535VLFMV

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: Medi Care System S.L.U.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 843603535VLFMV
Device name: Sujeción para pacientes en quirófano
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medi Care System S.L.U.
SRN: ES-MF-000008420
Country: Spain
Email: info@medisystemsl.com
Phone: 937570048

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPT6QMN985V1W6Z330FNARVT

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

VLF902008436035352746
VLF901008435489605286
VLF901208435489605316
VLF901108435489605309