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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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Kinesiology Tape — 10 UDI-DI variants, MDR

MD Atlas
Pro Dimi Healthcare GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Kinesiology Tape

42603601301100CL

10 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: Pro Dimi Healthcare GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42603601301100CL
Device name: Kinesiology Tape
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Pro Dimi Healthcare GmbH & Co. KG
SRN: DE-MF-000005539
Country: Germany
Email: susanne.saurin@mds-holding.de
Phone: 0231973525

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01FYV67CXEJ3S59FERTMS9A31F

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

Kinesiology Tape04260360130069
0426036013010604260360130106
0426036013012004260360130120
0426036013013704260360130137
0426036013011304260360130113
0426036013008304260360130083
0426036013009004260360130090
0426036013007604260360130076
Kinesiology Tape04260360130052
0426036013015104260360130151