Constant progesterone test reagent
Taiwan·Risk Class 2·DIAGNOSTIC SYSTEMS LABORATORIES, INC.·Registered Jan 26, 2006 – Jan 26, 2011Cancelled- Analysis ID
- 7eae0e676527e0184f4547e1b9c58e8a
- Customs Code
- DHAS0601595001
- Manufacturer
- DIAGNOSTIC SYSTEMS LABORATORIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WOLCH ENTERPRISES INC.
- Intended Use
- Radioimmunoassay quantification is used to detect yellow lipone monhormones in serum or blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1620 Progesterone testing system
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
- Registration Date
- Jan 26, 2006
- Expiry Date
- Jan 26, 2011
- Cancellation Date
- Nov 26, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for Constant progesterone test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7eae0e676527e0184f4547e1b9c58e8a and manufactured by DIAGNOSTIC SYSTEMS LABORATORIES, INC.. The authorized representative in Taiwan is WOLCH ENTERPRISES INC..
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