Taiwan FDA registration 076a156a2078d98aa33e0e3164fe793e
FLEXI-AID COLD/HOT PACK (Non-Sterile)
TW: 菲德 冷熱敷墊 (未滅菌)
Taiwan·Risk Class 1·MD·TAIWAN STANCH CO., LTD.·Registered May 06, 2019 – May 06, 2024CancelledRegistration details
- Analysis ID
- 076a156a2078d98aa33e0e3164fe793e
- License Form
- Ministry of Health Medical Device Manufacturing No. 007752
Company information
- Manufacturer
- TAIWAN STANCH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN STANCH CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5700 Medical Cold Pack
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 06, 2019
- Expiry Date
- May 06, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for FLEXI-AID COLD/HOT 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 076a156a2078d98aa33e0e3164fe793e and manufactured by TAIWAN STANCH CO., LTD.. The authorized representative in Taiwan is TAIWAN STANCH CO., LTD..
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