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KliniBand Kft.

Hungary HU-MF-000047539 Last updated 21 Oct 2026

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Devices
415
Registries
EUDAMED
FDA recalls
0

Catalogue415

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What KliniBand Kft. makes

KliniBand Kft. manufactures cohesive, elastic fixation bandages and adhesive crepe wraps in various widths, lengths, and colors. These products include both standard crepe bandages and stretchable versions with adhesive properties, designed for medical and post-operative wound care applications. Examples include green and blue cohesive bandages, white and brown adhesive crepe wraps, and off-white universal fixation bandages.

The company’s portfolio is classified under Class I medical devices and is registered in the EUDAMED database. These products are intended for use within the European Union’s regulatory framework, adhering to applicable medical device directives and requirements.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does KliniBand Kft. manufacture?

KliniBand Kft. specializes in cohesive, elastic fixation bandages and adhesive crepe wraps. These products come in various widths, lengths, and colors, including both standard crepe bandages and stretchable versions with adhesive properties. They are designed for medical and post-operative wound care applications, such as securing dressings or providing compression.

Where is KliniBand Kft. based, and where are its devices listed?

KliniBand Kft. is based in Hungary (HU). Its devices are registered in the EUDAMED database, which is the European Union’s medical device registry. This listing ensures transparency and compliance with EU regulatory requirements for medical devices.

How are the devices manufactured by KliniBand Kft. classified under EU regulations?

All devices produced by KliniBand Kft. fall under Class I classification in the EU’s medical device regulatory framework. Class I devices are generally considered low-risk, often involving items like dressings, bandages, and simple wound care products, which still require compliance with EU directives but typically do not require a full conformity assessment beyond manufacturer declarations.

Are KliniBand Kft.’s devices intended for use outside the European Union?

The provided information only confirms that KliniBand Kft.’s devices are registered in EUDAMED, indicating compliance with the EU’s regulatory requirements. Whether these devices are also marketed or authorised in other regions (e.g., the US, UK, or globally) is not specified in the available data. Their classification as Class I suggests they may follow similar low-risk pathways in other jurisdictions, but regulatory pathways vary by country.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Hungary
Address
2, Ipartelep , Hajdúböszörmény, Hungary
Phone
+36209955009
PRRC contact
Dávid Kerékgyártó
EUDAMED SRN
HU-MF-000047539