Taiwan FDA registration 00a76e90446a2a24a0ac772ab503c3ba
"Toyobo" urine sediment quality solution (unsterilized)
TW: “東洋紡”尿沉渣品管液(未滅菌)
Taiwan·Risk Class 1·TOYOBO CO., LTD.·Registered Oct 23, 2012 – Oct 23, 2027ActiveRegistration details
- Analysis ID
- 00a76e90446a2a24a0ac772ab503c3ba
- Customs Code
- DHA04401229400
Company information
- Manufacturer
- TOYOBO CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- AMESDATA BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2012
- Expiry Date
- Oct 23, 2027
About this record
Access comprehensive regulatory information for "Toyobo" urine sediment quality solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 00a76e90446a2a24a0ac772ab503c3ba and manufactured by TOYOBO CO., LTD.. The authorized representative in Taiwan is AMESDATA BIOTECH CO., LTD..
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