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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 800 — 7 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 800

805773712FT71MBS

7 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: 805773712FT71MBS
Device name: —
Device model: Moviplan 800
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 22, 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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FN42G4D2PRDBQ8F50GAY6WSW

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

977110070308057737122644
977110080308057737122651
977110030308057737122620
977110040308057737122637
977110110308057737122675
977111110308057737122682
977110090308057737122668