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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 Crepp Haft — 106 UDI-DI variants, MDR (KliniBand Kft.)

MD Atlas
KliniBand Kft.

Data from EUDAMED, last updated May 24, 2026

Klini Crepp Haft

59991482KB101RT

106 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: 59991482KB101RT
Device name: Klini Crepp Haft
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 27, 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

106 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JYR2Q59ZQ2VXBMWQ0BM90MG6

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

90241005999148224001
90240405999148223905
90240605999148223967
90240805999148223547
Salus Cohesive 10 cm x 4 m05999148223189
Salus Cohesive 12 cm x 4 m05999148223196

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