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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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Klini Flex — 29 UDI-DI variants, MDR (KliniBand Kft.)

MD Atlas
KliniBand Kft.

Data from EUDAMED, last updated May 24, 2026

Klini Flex

59991482KB03WN

29 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: KliniBand Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59991482KB03WN
Device name: Klini Flex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: KliniBand Kft.
SRN: HU-MF-000047539
Country: Hungary
Email: david.kerekgyarto@kliniband.com
Phone: +36209955009

Variants by status

UDI-DI variants

29 UDI-DI variants

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Applied filters

basicUdiUlid01JZWWZ275474TK4B6DCGJ1K17

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

Klini Flex 8cmx4m brown05999148203082
Klini Flex 8cmx4m brown KLP05999148203099
Klini Flex 8cmx4m white05999148202887
Klini Flex 8cmx4m white KLP05999148202894

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