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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-Sonic — 3 UDI-DI variants, MDR (KIRMED INTERNATIONAL SRL)

MD Atlas
KIRMED INTERNATIONAL SRL

Data from EUDAMED, last updated May 31, 2026

K-Sonic

805977296KSOUT

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: KIRMED INTERNATIONAL SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805977296KSOUT
Device name: —
Device model: K-Sonic
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: KIRMED INTERNATIONAL SRL
SRN: IT-MF-000035071
Country: Italy
Email: info@kirmedinternational.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSME4AA6BFA69ZQM0QXEM4RE

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-Sonic Dental electromedical system console08059772960045
K-Sonic I.Son electromedical system console08059772960038
K-Sonic2 electromedical system console08059772960021