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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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K•BOX — 1 UDI-DI variant, MDR (Drop Digital Health S.r.l.)

MD Atlas
Drop Digital Health S.r.l.

Data from EUDAMED, last updated May 31, 2026

K•BOX

0805363013BOX_KBOXUN

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 Digital Health S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0805363013BOX_KBOXUN
Device name: K•BOX
Device model: K•HERO K•BOX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: Drop Digital Health S.r.l.
SRN: IT-MF-000046691
Country: Italy
Email: david.ferrini@dropdigitalhealth.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JMYF8GVG3HP08R7JZX9CSEPC

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

K•BOX08053630130014