Taiwan FDA registration 566d21962f0d511daec87ec7d6fd0dc6
Constant luteinizing gonadotropin immunoassay group
TW: 常盈黃體促素免疫試劑組
Taiwan·Risk Class 1·DIAGNOSTIC SYSTEMS LABORATORIES, INC.·Registered May 16, 2006 – May 16, 2011CancelledRegistration details
- Analysis ID
- 566d21962f0d511daec87ec7d6fd0dc6
- Customs Code
- DHA04400450201
Company information
- Manufacturer
- DIAGNOSTIC SYSTEMS LABORATORIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WOLCH ENTERPRISES INC.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2006
- Expiry Date
- May 16, 2011
- Cancellation Date
- Nov 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Constant luteinizing gonadotropin immunoassay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 566d21962f0d511daec87ec7d6fd0dc6 and manufactured by DIAGNOSTIC SYSTEMS LABORATORIES, INC.. The authorized representative in Taiwan is WOLCH ENTERPRISES INC..
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