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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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Plantari semilavorati Linea Cuoio — 1 UDI-DI variant, MDR

MD Atlas
Plantamed società a responsabiltà limitata

Data from EUDAMED, last updated May 31, 2026

Plantari semilavorati Linea Cuoio

8051554010115UL

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Plantamed società a responsabiltà limitata

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8051554010115UL
Device name: Plantari semilavorati Linea Cuoio
Device model: Plantari semilavorati Linea Cuoio
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Plantamed società a responsabiltà limitata
SRN: IT-MF-000050705
Country: Italy
Email: info@plantamed.it
Phone: +390679815309

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQW4SW3DD0XWET5Q4Q9ZVA3A

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

235651008051554010115