Taiwan FDA registration 3d6a2e1c54e5ec52109fd23497794253

"Kinestica" Continuous Passive Motion Device (Non-Sterile)

TW: "金斯提卡" 連續式被動關節活動器 (未滅菌)

Taiwan·Risk Class 1·MD·KINESTICA D.O.O.·Registered Jul 30, 2018 – Jul 30, 2023Expired

Registration details

Analysis ID: 3d6a2e1c54e5ec52109fd23497794253
License Form: Ministry of Health Medical Device Import No. 019428
Customs Code: DHA09401942800

Company information

Manufacturer: KINESTICA D.O.O.
Manufacturer Country: Slovenia
Authorized Representative: SCHMIDT SCIENTIFIC TAIWAN LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O0006 Continuous Passive Joint Activator
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 30, 2018
Expiry Date: Jul 30, 2023

About this record

Access comprehensive regulatory information for "Kinestica" Continuous Passive Motion Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3d6a2e1c54e5ec52109fd23497794253 and manufactured by KINESTICA D.O.O.. The authorized representative in Taiwan is SCHMIDT SCIENTIFIC TAIWAN LTD..

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