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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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PARKINSON REHAB® — 1 UDI-DI variant, MDR (DROP S.R.L.S.)

MD Atlas
DROP S.R.L.S.

Data from EUDAMED, last updated May 30, 2026

PARKINSON REHAB®

805071454SW_PARKINSONRE3P

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: DROP S.R.L.S.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805071454SW_PARKINSONRE3P
Device name: PARKINSON REHAB®
Device model: PARKINSON REHAB®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Oct 25, 2023

Manufacturer & authorised representative

Manufacturer

Name: DROP S.R.L.S.
SRN: IT-MF-000021294
Country: Italy
Email: amministrazione@dropsolution.it
Phone: +39 069641506

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HDK6PVXY2QG4Y4SDGRCX2VS4

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

PARKINSON REHAB®08050714540042