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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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MIA HAND — 8 UDI-DI variants, MDR (Prensilia SRL)

MD Atlas
Prensilia SRL

Data from EUDAMED, last updated May 30, 2026

MIA HAND

805227819MIAHANDKY

8 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: Prensilia SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805227819MIAHANDKY
Device name: MIA HAND
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Prensilia SRL
SRN: IT-MF-000027917
Country: Italy
Email: info@prensilia.com
Phone: +390587274826

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HVK5GWARR27ECYQ7HS3GWW6A

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

Non Sensorized Left Prosthesis Mia Hand08052278190077
Non-sensorized Left Prosthesis Mia Hand08052278190039
Non-sensorized Right Prosthesis Mia Hand08052278190015
Non-Sensorized Right Prosthesis Mia Hand08052278190053
Sensorized Left Prosthesis Mia Hand08052278190060
Sensorized Left Prosthesis Mia Hand08052278190022
Sensorized Right Prosthesis Mia Hand08052278190008
MI-100000-0108052278190046