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Kinesiology Tape - EUDAMED Registration 08032764682040

Access comprehensive regulatory information for Kinesiology Tape in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 08032764682040 and manufactured by Atex Co., Ltd in Republic of Korea.

This page provides complete registration details including trade name (DREAM K), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class I
08032764682040
No
Kinesiology Tape
Trade Name: DREAM K
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Device Description (EMDN)

TAPES, MEDICAL/SURGICAL - OTHER

Device Classification
Risk Class
Class I
CND Nomenclatures Code
H900299
Trade Name
DREAM K
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08032764682040
Basic UDI
80327646820402S
Version Date
March 04, 2025
Manufacturer Last Update
August 27, 2021
Active Status
No
Manufacturer
Manufacturer Name
Atex Co., Ltd
Country
Republic of Korea
Country Type
NON_EU
Address
144 Jangjisan-ro Paju-si
Email
atexsales@atexmedical.com
Authorized Representative
SRN
IE-AR-000004258
Country
Ireland
Address
Unit 3D North Point House North Point Business Park New Mallow Road Cork
Email
ar@meridiusmedical.com
Telephone
+353 212066448
Regulatory Information
Competent Authority
Health Products Regulatory Authority, Medical Devices Department
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Italy
Device Characteristics
Human Tissues
No
Animal Tissues
No