Taiwan FDA registration e5deb9fe14acc1a6365c6b808e3b5cdf
"Siemens" basic phosphoric acid per (AMP method) reagent set
TW: “西門子”鹼性磷酸每(AMP法)試劑組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Jan 22, 2008 – Jan 22, 2018CancelledRegistration details
- Analysis ID
- e5deb9fe14acc1a6365c6b808e3b5cdf
- Customs Code
- DHA00601893101
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For in vitro diagnostics. The activity of basic phosphoric acid in human serum and plasma was quantitatively determined on the ADVIA fully automated chemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1050 Alkaline phosphatase or isoenzyme testing system
- Import Information
- import
Dates and status
- Registration Date
- Jan 22, 2008
- Expiry Date
- Jan 22, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" basic phosphoric acid per (AMP method) reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5deb9fe14acc1a6365c6b808e3b5cdf and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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