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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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BUDDYCARE® MED Kine-Tape — 4 UDI-DI variants, MDR (Bugslock GmbH)

MD Atlas
Bugslock GmbH

Data from EUDAMED, last updated May 23, 2026

BUDDYCARE® MED Kine-Tape

0912005044KineTape01N5

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Bugslock GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0912005044KineTape01N5
Device name: BUDDYCARE® MED Kine-Tape
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: Bugslock GmbH
SRN: AT-MF-000046984
Country: Austria
Email: info@bugslock.at
Phone: +43 1 236 1919

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JRCZMYYFCCN3DCBRTN640071

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

2023271AR09120050442504
2023272AR09120050442511
2023274AR09120050442535
2023273AR09120050442528