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"Tienovi" torso equipment (unsterilized) - Taiwan Registration d353e10c362584a12616b2e0807679ab

Access comprehensive regulatory information for "Tienovi" torso equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d353e10c362584a12616b2e0807679ab and manufactured by TECNOWAY S.R.L.. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING CO., LTD..

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d353e10c362584a12616b2e0807679ab
Registration Details
Taiwan FDA Registration: d353e10c362584a12616b2e0807679ab
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Device Details

"Tienovi" torso equipment (unsterilized)
TW: "้ต่ซพๅจ" ่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d353e10c362584a12616b2e0807679ab

DHA08401940209

Company Information

Italy

Product Details

Limited to the first level identification scope of the "Torso Equipment (O.3490)" classification and grading management measures for medical equipment.

o Physical Medical Sciences

O.3490 Torso mounting

import

Dates and Status

Oct 01, 2021

Oct 31, 2025