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Bugslock GmbH

Austria AT-MF-000046984 Last updated 21 Oct 2026

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Devices
23
Registries
EUDAMED
FDA recalls
0

Catalogue23

About

Practical solutions for everyday life – developed with responsibility At Bugslock, we develop, manufacture and distribute well-designed products and private label solutions – including those in the medical sector. Working closely with experts from various disciplines, we create solutions that simplify daily life and meet real needs. From the initial idea to market launch, we

From the manufacturer's own website. Source

What Bugslock GmbH makes

Bugslock GmbH manufactures medical-grade kinesiology tapes and bandages, including colored and specialized tapes for fingers (e.g., purple, blue, yellow, and camouflage green), as well as adhesive bandages and sport-specific tapes in white and red. These products are designed for temporary skin support, injury recovery, and athletic performance applications.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class I devices and is registered in the EU’s eudamed database. Bugslock GmbH is based in Austria.

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 Bugslock GmbH manufacture?

Bugslock GmbH specializes in medical-grade kinesiology tapes and bandages. Their portfolio includes specialized finger tapes (available in colors like purple, blue, yellow, and camouflage green), adhesive bandages, and sport-specific tapes such as white and red sport-tape. These products are designed for temporary skin support, injury recovery, and athletic performance applications, ensuring practical solutions for everyday medical and sports needs.

Where is Bugslock GmbH based, and how does this affect its regulatory standing?

Bugslock GmbH is based in Austria, which means its medical devices must comply with the European Union’s regulatory framework. Since their products fall under the EU Medical Device Regulation (MDR), they are classified as Class I devices, indicating a lower risk profile. Their devices are registered in the EU’s official database, eudamed, which tracks authorized medical devices within the European Economic Area.

Which regulatory registries list Bugslock GmbH’s devices, and why is this important?

Bugslock GmbH’s devices are listed in eudamed, the European Union’s central database for medical devices. This registry ensures transparency and traceability of authorized products within the EU, allowing healthcare professionals, regulators, and patients to verify compliance with EU Medical Device Regulation (MDR) requirements. Listing in eudamed confirms that the devices meet necessary safety, performance, and regulatory standards before entering the market.

How are Bugslock GmbH’s devices classified under EU regulations, and what does this classification mean?

Bugslock GmbH’s devices are classified as Class I under the EU Medical Device Regulation (MDR). This classification applies to low-risk products, such as medical-grade tapes and bandages, which pose minimal risk to patients. Class I devices typically require general safety and performance requirements to be met but do not always need pre-market notification or third-party involvement, though compliance with MDR obligations (e.g., labeling, traceability) remains mandatory.

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

Information

Country
Austria
Address
106, St. Stefan, Globasnitz, Austria
Phone
+43 1 236 1919
PRRC contact
Thomas Thonhofer
EUDAMED SRN
AT-MF-000046984