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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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Organization name
UDI-DI code
Reference / catalog number

2023271AR — Class I MDR by Bugslock GmbH

MD Atlas
Bugslock GmbH

EUDAMED last updated this device on Apr 9, 2025

2023271AR

0912005044KineTape01N5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bugslock GmbH
UDI-DI code: 09120050442504
Reference / catalog number: 2023271AR

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Manufacturer information

Organization name: Bugslock GmbH
SRN: AT-MF-000046984
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Germany		Still on market

Device identification

Trade name: not provided
UDI-DI code: 09120050442504
Basic UDI-DI: 0912005044KineTape01N5
Reference / catalog number: 2023271AR
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: Elastisches, hautfreundliches Kinesiologie-Tape für therapeutische Anwendungen. Unterstützt die Stabilisierung von Muskeln und Gelenken, fördert die Beweglichkeit und kann Schmerzen lindern. Latexfrei, luftdurchlässig und bis zu 160 % dehnbar. Geeignet zur Anwendung bei Muskelverspannungen, zur Durchblutungsförderung sowie zur Entlastung bei Verletzungen im Bewegungsapparat. In wiederverschließbarer Hygieneverpackung.
Additional information URL: https://buddycare.eu/BUDDYCARE-MED-Kine-Tape-BLAU-5cm-x-5m-Latexfrei
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030402030102ELASTIC SUPPORT BANDAGES, ADHESIVE EXTENSIBLE IN ONE DIRECTION, HIGH EXTENSIBILITY

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
Expiration date
Manufacturing date
Serial number
Software identification

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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.