Taiwan FDA registration 2d174070e911ffd9521bf40df8941748

"Siemens" Automatic Chemical Analysis System Reagent Probe Cleaning Solution 2 (Unsterilized)

TW: “西門子”全自動化學分析系統試劑探針清洗液2 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Oct 23, 2007 – Oct 23, 2017Cancelled
Registration details
Analysis ID
2d174070e911ffd9521bf40df8941748
Customs Code
DHA04400624208
Company information
Manufacturer Country
United States;;Japan
Authorized Representative
SIEMENS LIMITED
Product details
Intended Use
Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.4010 Reaction Reagents for General Purposes
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Oct 23, 2007
Expiry Date
Oct 23, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Siemens" Automatic Chemical Analysis System Reagent Probe Cleaning Solution 2 (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d174070e911ffd9521bf40df8941748 and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices