Taiwan FDA registration 4e7f5cfbc5b02fc0f8d446bf7fcfbca7

"Siemens" 2400 Biochemical Analyzer (Unsterilized)

TW: "西門子"2400生化分析儀 (未滅菌)

Taiwan·Risk Class 1·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Aug 21, 2008 – Aug 21, 2018Cancelled

Registration details

Analysis ID: 4e7f5cfbc5b02fc0f8d446bf7fcfbca7
Customs Code: DHA04400701107

Company information

Manufacturer: JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States;;Japan
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Aug 21, 2008
Expiry Date: Aug 21, 2018
Cancellation Date: May 19, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Siemens" 2400 Biochemical Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4e7f5cfbc5b02fc0f8d446bf7fcfbca7 and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE 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.