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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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Mover — 11 UDI-DI variants, MDR

MD Atlas
KOVAL PROIZVODNJA IN TRGOVINA, D.O.O.

Data from EUDAMED, last updated May 31, 2026

Mover

383007592KV26AA

11 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: KOVAL PROIZVODNJA IN TRGOVINA, D.O.O.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 383007592KV26AA
Device name: Mover
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: KOVAL PROIZVODNJA IN TRGOVINA, D.O.O.
SRN: SI-MF-000003206
Country: Slovenia
Email: koval@koval.si
Phone: +386 3 747 19 14

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGKRRXEZJAJ0JXGCYN17JGTS

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

1199212103830075920821
1199214503830075920845
1199215003830075923228
1199215103830075924133
1199214603830075923396
1199212303830075920838
1199212403830075923402
1199218203830075920869
1199218203830075920876
1199218203830075920852
1199214703830075924652