Taiwan FDA registration 685c455c894dbbd797019767eab5820b
"Hengyang" warm patch (unsterilized)
TW: "恆陽" 溫熱貼 (未滅菌)
Registration details
- Analysis ID
- 685c455c894dbbd797019767eab5820b
Company information
- Manufacturer
- VENICE LABORATORIES CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SOLARIS BIOPHARMA CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5710 醫療用可丟棄式的冷熱敷包
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Aug 23, 2016
- Expiry Date
- Aug 23, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Hengyang" warm patch (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 685c455c894dbbd797019767eab5820b and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is SOLARIS BIOPHARMA 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.
Free DatabasePowered by Pure Global AI89,000+ Devices