Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

2017173AR — Class I MDR by Bugslock GmbH

MD Atlas
Bugslock GmbH

EUDAMED last updated this device on Oct 31, 2025

2017173AR

0912005044FINGER-TAPE01UU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bugslock GmbH
UDI-DI code: 09120050442382
Reference / catalog number: 2017173AR

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

2017166AR0912005044FINGER-TAPE01UUOn the market 2017167AR0912005044FINGER-TAPE01UUOn the market 2017170AR0912005044FINGER-TAPE01UUOn the market 2017168AR0912005044FINGER-TAPE01UUOn the market 2017169AR0912005044FINGER-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.

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: 09120050442382
Basic UDI-DI: 0912005044FINGER-TAPE01UU
Reference / catalog number: 2017173AR
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