Taiwan FDA registration f5884425cc3d24ca5277dfce7c5d09df
“J.P.”Cushion (Non-Sterile)
TW: “建鵬”浮動坐墊 (未滅菌)
Taiwan·Risk Class 1·MD·SEALTECH., LTD·Registered Apr 12, 2017 – Apr 12, 2022ExpiredRegistration details
- Analysis ID
- f5884425cc3d24ca5277dfce7c5d09df
- License Form
- Ministry of Health Medical Device Import No. 017703
- Customs Code
- DHA09401770309
Company information
- Manufacturer
- SEALTECH., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- J. P. 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
- Imported from abroad
Dates and status
- Registration Date
- Apr 12, 2017
- Expiry Date
- Apr 12, 2022
About this record
Access comprehensive regulatory information for “J.P.”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 f5884425cc3d24ca5277dfce7c5d09df and manufactured by SEALTECH., LTD. The authorized representative in Taiwan is J. P. CO., LTD..
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