Taiwan FDA registration 70c9bfe7164edadfcb325dc0d7abc5db
“Mammy Village” Cold Pack (Non-Sterile)
TW: “六甲村”冷敷袋 (未滅菌)
Taiwan·Risk Class 1·MD·MAMMY VILLAGE CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- 70c9bfe7164edadfcb325dc0d7abc5db
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 002593
- Customs Code
- DHY08300259300
Company information
- Manufacturer
- MAMMY VILLAGE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MAMMY VILLAGE 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 “Mammy Village” 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 70c9bfe7164edadfcb325dc0d7abc5db and manufactured by MAMMY VILLAGE CO., LTD.. The authorized representative in Taiwan is MAMMY VILLAGE CO., LTD..
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