Taiwan FDA registration 2c2cb8996b9a5a5c711949be0c85d669
LUMIPULSE G1200 (Non-Sterile)
TW: 錄秘帕斯G1200 化學冷光儀(未滅菌)
Taiwan·Risk Class 1·MD·OTSUKA ELECTRONICS CO., LTD. SHIGA FACTORY·Registered Oct 01, 2021 – Oct 31, 2026CancelledRegistration details
- Analysis ID
- 2c2cb8996b9a5a5c711949be0c85d669
- License Form
- Ministry of Health Medical Device Import Registration No. 009828
- Customs Code
- DHA08400982801
Company information
- Manufacturer
- OTSUKA ELECTRONICS CO., LTD. SHIGA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- Taiwan Fu Pharmaceutical Co., Ltd
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2160 Individual photometric chemistry analyzer for clinical use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
- Cancellation Date
- Oct 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for LUMIPULSE G1200 (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 2c2cb8996b9a5a5c711949be0c85d669 and manufactured by OTSUKA ELECTRONICS CO., LTD. SHIGA FACTORY. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
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