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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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Moviplan iC — 56 UDI-DI variants, MDR (Villa Sistemi Medicali S.p.A.)

MD Atlas
Villa Sistemi Medicali S.p.A.

Data from EUDAMED, last updated May 30, 2026

Moviplan iC

805773712FT2369T

56 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: Villa Sistemi Medicali S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805773712FT2369T
Device name: Moviplan iC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 3, 2021

Manufacturer & authorised representative

Manufacturer

Name: Villa Sistemi Medicali S.p.A.
SRN: IT-MF-000016860
Country: Italy
Email: qa@villasm.com

Variants by status

UDI-DI variants

56 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FP04YY715SK8DZVEFY2S7CNG

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

978910723008057737123009
978910201008057737122866
978910224008057737122880
978910701008057737122996
978910724008057737123016
978900212008057737122767

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