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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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Carrozzine manuali ad autospinta… — 35 UDI-DI variants, MDR

MD Atlas
GIALDI S.R.L.

Data from EUDAMED, last updated May 31, 2026

Carrozzine manuali ad autospinta posteriore

80541102700KE

35 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: 80541102700KE
Device name: Carrozzine manuali ad autospinta posteriore
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 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

35 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKY0BG11VE487PN4AAMGFXTJ

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

11045308054110271449
11045408054110271456
11045508054110271463
11045608054110271470
11045708054110271487
110457.HD08054110271623
11045808054110271494
110458.HD08054110271630
11045908054110271500
110459.HD08054110271647

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