Taiwan FDA registration 887c0f6bf3c4607e9768eb774a53adf4
Bioresearch liquid correction solution
TW: 生研液狀校正液
Taiwan·Risk Class 2·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Dec 20, 2005 – Dec 20, 2025CancelledRegistration details
- Analysis ID
- 887c0f6bf3c4607e9768eb774a53adf4
- Customs Code
- DHA00601569704
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- It is used to establish a reference point in the test reagent to determine the measured value of the substance in the human sample.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 2005
- Expiry Date
- Dec 20, 2025
- Cancellation Date
- Jul 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Bioresearch liquid correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 887c0f6bf3c4607e9768eb774a53adf4 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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