Taiwan FDA registration b38c0d8f326feff1a5a4639e8fd81ee9
OPPO Cold/Hot Pack (Non-sterile)
TW: OPPO冷熱敷包 (未滅菌)
Taiwan·Risk Class 1·MD·PLUS MEDITECH CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- b38c0d8f326feff1a5a4639e8fd81ee9
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 004940
Company information
- Manufacturer
- PLUS MEDITECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PLUS MEDITECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for OPPO 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 b38c0d8f326feff1a5a4639e8fd81ee9 and manufactured by PLUS MEDITECH CO., LTD.. The authorized representative in Taiwan is PLUS MEDITECH CO., LTD..
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