Taiwan FDA registration f8d40b480e826d9b74143862b64565a4
SENTEQ Flotation cushion (non-sterile)
TW: 登康美 浮動坐墊 (未滅菌)
Registration details
- Analysis ID
- f8d40b480e826d9b74143862b64565a4
- License Form
- Ministry of Health Medical Device Manufacturing No. 006546
Company information
- Manufacturer
- SENTEQ CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SENTEQ CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3175 floating seat cushion
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 30, 2016
- Expiry Date
- Dec 30, 2026
About this record
Access comprehensive regulatory information for SENTEQ Flotation cushion (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 f8d40b480e826d9b74143862b64565a4 and manufactured by SENTEQ CO., LTD.. The authorized representative in Taiwan is SENTEQ CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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