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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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Dispositivo antidecubito in lana — 3 UDI-DI variants, MDR

MD Atlas
BANCHI MAISON S.R.L.

Data from EUDAMED, last updated May 31, 2026

Dispositivo antidecubito in lana

8050714610000LAC4

3 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: BANCHI MAISON S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8050714610000LAC4
Device name: Dispositivo antidecubito in lana
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: BANCHI MAISON S.R.L.
SRN: IT-MF-000031460
Country: Italy
Email: info@maisonbanchi.com
Phone: + 39 0573 55108

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSJG4PZ2GBAPWXE20AERHBT1

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

LA001 10108050714610066
LA001 15008050714610073
LA001 5010008050714610288