Taiwan FDA registration 6c294bc9147529209b4ce18c570d03aa
"Kinetec" Water circulating hot or cold pack (Non-Sterile)
TW: "肯尼帝克" 醫療用水循環式冷熱敷包 (未滅菌)
Taiwan·Risk Class 1·MD·KINETEC SAS·Registered Mar 21, 2016 – Mar 21, 2021ExpiredRegistration details
- Analysis ID
- 6c294bc9147529209b4ce18c570d03aa
- License Form
- Ministry of Health Medical Device Import No. 016283
- Customs Code
- DHA09401628308
Company information
- Manufacturer
- KINETEC SAS
- Manufacturer Country
- France
- Authorized Representative
- BLESSING CATHAY CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Medical Water Recycling Hot and Cold Compress Pack (O.5720)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5720 Medical Water Recycling Hot and Cold Pack
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 21, 2016
- Expiry Date
- Mar 21, 2021
About this record
Access comprehensive regulatory information for "Kinetec" Water circulating hot or cold pack (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 6c294bc9147529209b4ce18c570d03aa and manufactured by KINETEC SAS. The authorized representative in Taiwan is BLESSING CATHAY CORPORATION.
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