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Artemis Series Electric Surgical Table - EUDAMED Registration 04719879260908

Access comprehensive regulatory information for Artemis Series Electric Surgical Table 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 04719879260908 and manufactured by Mediland Enterprise Corporation in Taiwan.

This page provides complete registration details including trade name (Artemis), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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
04719879260908
Yes
Artemis Series Electric Surgical Table
Trade Name: Artemis
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Device Description (EMDN)

OPERATING TABLES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Z12011202
Trade Name
Artemis
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
04719879260908
Basic UDI
471987926ArtemisAA
Version Date
November 15, 2024
Manufacturer Last Update
May 16, 2022
Active Status
Yes
Manufacturer
Country
Taiwan
Country Type
NON_EU
Address
No.75, Wenhwa 1st Rd, Taoyuan City
Email
leo_pan@mediland.com.tw
Authorized Representative
SRN
NL-AR-000002750
Country
Netherlands
Address
18 Abtswoudseweg Delft
Email
info@luanamed.com
Telephone
+31152220009
Regulatory Information
Competent Authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Netherlands
Device Characteristics
Human Tissues
No
Animal Tissues
No