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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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Deambulatori a ruote — 15 UDI-DI variants, MDR (GIALDI S.R.L.)

MD Atlas
GIALDI S.R.L.

Data from EUDAMED, last updated May 30, 2026

Deambulatori a ruote

80541102709KY

15 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: GIALDI S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80541102709KY
Device name: Deambulatori a ruote
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: GIALDI S.R.L.
SRN: IT-MF-000048723
Country: Italy
Email: info@gialdi.it
Phone: +39 0522 975118

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KS5JHHFJ9E7R677Y31GEXDX1

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

20135008054110271999
20135108054110272002
20135208054110272019
20135308054110272026
20135808054110272064
20135608054110272040
20135508054110272033
20135708054110272057
20145208054110270718
20145308054110270725
20144408054110270701
20145508054110271708
20200008054110271531
20106008054110270916
20104008054110270435