Taiwan FDA registration 10ab70e7b36ad3ac19ede52204f6482c
"Medical Sincerity" Serum Out-of-Hospital Quality Control Program (Unsterilized)
TW: "醫誠"血清院外品管計劃 (未滅菌)
Taiwan·Risk Class 1·RANDOX LABORATORIES LTD.·Registered May 08, 2013 – May 08, 2018CancelledRegistration details
- Analysis ID
- 10ab70e7b36ad3ac19ede52204f6482c
- Customs Code
- DHA04401299201
Company information
- Manufacturer
- RANDOX LABORATORIES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A1660) of the Measures for the Administration of Medical Devices.
- 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
- May 08, 2013
- Expiry Date
- May 08, 2018
- Cancellation Date
- Nov 28, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medical Sincerity" Serum Out-of-Hospital Quality Control Program (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 10ab70e7b36ad3ac19ede52204f6482c and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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