Bugslock GmbH
Austria AT-MF-000046984 Last updated 21 Oct 2026
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- Devices
- 23
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
BUDDYCARE® MED Sport-Tape Weiss Ref 2023268AR
BUDDYCARE® MED Pflasterbandagen Rot Ref 2020217AR
BUDDYCARE® MED Pflasterbandagen Haut Ref 2020216AR
BUDDYCARE® MED Kine-Tape Blau Ref 2023271AR
Buddycare® Med Finger-Tape Purpur Ref 2017174AR
Buddycare® Med Finger-Tape Blau Ref 2017166AR
Buddycare® Med Finger-Tape Gelb Ref 2017167AR
BUDDYCARE® MED Sport-Tape Rot Ref 2023267AR
BUDDYCARE® MED FINGER-TAPE Gras Grün Ref 2017170AR
BUDDYCARE® MED Pflasterbandage Blau Ref 2020215AR
Buddycare® Med Finger-Tape Hautfarben Ref 2017169AR
BUDDYCARE® MED Pflasterbandagen Camouflage Grün Ref 2020219AR
BUDDYCARE® MED Kine-Tape Haut Ref 2023272AR
BUDDYCARE® MED Sport-Tape Blau Ref 2023265AR
BUDDYCARE® MED Sport-Tape Schwarz Ref 2023266AR
Buddycare® Med Finger-Tape Rot Ref 2017172AR
Buddycare® Med Finger-Tape Grün Ref 2017168AR
Buddycare® Med Finger-Tape Pink Ref 2017171AR
BUDDYCARE® MED Kine-Tape Pink Ref 2023274AR
BUDDYCARE® MED Kine-Tape Schwarz Ref 2023273AR
BUDDYCARE® MED Pflasterbandagen Schwarz Ref 2020218AR
Buddycare® Med Finger-Tape Schwarz Ref 2017173AR
BUDDYCARE® MED Pflasterbandagen Camouflage Pink Ref 2020220AR
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
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.
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.
Information
- Country
- Austria
- Address
- 106, St. Stefan, Globasnitz, Austria
- Website
- www.bugslock.at
- [email protected]
- Phone
- +43 1 236 1919
- PRRC contact
- Thomas Thonhofer
- EUDAMED SRN
- AT-MF-000046984