Taiwan FDA registration 539061fbd856fd772233d42f72043b46
“NISSEI” Fingertip Pulse Oximeter
TW: “日本精密”手指型血氧濃度計
Taiwan·Risk Class 2·MD·NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY·Registered Dec 01, 2021 – Dec 01, 2026ActiveRegistration details
- Analysis ID
- 539061fbd856fd772233d42f72043b46
- License Form
- Ministry of Health Medical Device Import No. 035045
- Customs Code
- DHA05603504505
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)
- E2700 Oximeter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 01, 2021
- Expiry Date
- Dec 01, 2026
About this record
Access comprehensive regulatory information for “NISSEI” Fingertip 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 539061fbd856fd772233d42f72043b46 and manufactured by NIHON SEIMITSU SOKKI CO., LTD., KOMOCHI FACTORY. The authorized representative in Taiwan is SUN-UP HEALTHCARE 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