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Organization name
UDI-DI code
Reference / catalog number

Klini Flex 6 cm x 4 m white — Class I MDR by KliniBand Kft.

MD Atlas
KliniBand Kft.

EUDAMED last updated this device on Jan 15, 2026

Klini Flex 6 cm x 4 m white

59991482KB03WN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: KliniBand Kft.
UDI-DI code: 05999148222878
Reference / catalog number: KB00310060040

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Manufacturer information

Organization name: KliniBand Kft.
SRN: HU-MF-000047539
Manufacturer status: Active

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Hungary; available across 2 countries total.

Country	On market since	Until
HungaryPrimary placement		Still on market
Romania		Still on market

Device identification

Trade name: Klini Flex 6 cm x 4 m white
UDI-DI code: 05999148222878
Basic UDI-DI: 59991482KB03WN
Reference / catalog number: KB00310060040
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: elastic fixation bandage 6cmx4m white, cello.bulk
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 6 MU10
4 MU36

EMDN nomenclature code(s)

M0303010101ELASTIC FIXING BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
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