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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

2017170AR — Class I MDR by Bugslock GmbH

MD Atlas
Bugslock GmbH

EUDAMED last updated this device on Oct 31, 2025

2017170AR

0912005044FINGER-TAPE01UU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bugslock GmbH
UDI-DI code: 09120050442351
Reference / catalog number: 2017170AR

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Manufacturer information

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

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Intolerance to components. Arterial circulatory disorders. Severe sensory disturbances/neuropathies. Highly irritated/pre-damaged/infected skin. Directly on open wounds (only over a sterile dressing). For external use only. In case of redness, itching, pressure pain, numbness, or a cold sensation, remove immediately. Seek medical advice for persistent symptoms. For unclear/severe injuries, consult a doctor.

Market distribution

Primary placement in Austria; available across 1 country total.

Placed on the market in Austria; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 09120050442351
Basic UDI-DI: 0912005044FINGER-TAPE01UU
Reference / catalog number: 2017170AR
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 tape for finger and nail protection; securing of wound dressings; protection against friction, pressure spots, blisters
Additional information URL: https://buddycare-med.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030402020101ELASTIC SUPPORT BANDAGES, COHESIVE, 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

Related devices

2017166AR0912005044FINGER-TAPE01UUOn the market 2017167AR0912005044FINGER-TAPE01UUOn the market 2017168AR0912005044FINGER-TAPE01UUOn the market 2017169AR0912005044FINGER-TAPE01UUOn the market 2017171AR0912005044FINGER-TAPE01UUOn the market

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.