Taiwan FDA registration 6b3660852690cf32d06761d1b028fe2e
"Kiyokva" torso device (unsterilized)
TW: “奇優克瓦”軀幹裝具 (未滅菌)
Taiwan·Risk Class 1·KIYOKAWA CO., LTD.·Registered Jul 08, 2008 – Jul 08, 2018CancelledRegistration details
- Analysis ID
- 6b3660852690cf32d06761d1b028fe2e
- Customs Code
- DHA04400688307
Company information
- Manufacturer
- KIYOKAWA CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- PURIGO BIOTECH INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3490 Torso mounting
- Import Information
- import
Dates and status
- Registration Date
- Jul 08, 2008
- Expiry Date
- Jul 08, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Kiyokva" torso device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6b3660852690cf32d06761d1b028fe2e and manufactured by KIYOKAWA CO., LTD.. The authorized representative in Taiwan is PURIGO BIOTECH INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices