Taiwan FDA registration 3eeb93f201fad95ce4a127c299f3f49c
“Nissei” Digital Blood Pressure Monitor and Pulse oximeter
TW: “日本精密” 血壓/血氧濃度監測器
Taiwan·Risk Class 2·MD·NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY·Registered Jan 28, 2022 – Jan 28, 2027ActiveRegistration details
- Analysis ID
- 3eeb93f201fad95ce4a127c299f3f49c
- License Form
- Ministry of Health Medical Device Import No. 035148
- Customs Code
- DHA05603514802
Company information
- Manufacturer
- NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- SUN-UP HEALTHCARE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E1130 Non-invasive blood pressure measurement system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 28, 2022
- Expiry Date
- Jan 28, 2027
About this record
Access comprehensive regulatory information for “Nissei” Digital Blood Pressure Monitor and Pulse oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3eeb93f201fad95ce4a127c299f3f49c and manufactured by NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY. The authorized representative in Taiwan is SUN-UP HEALTHCARE CO., LTD..
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