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Taiwan FDA registration 55c70638948a7e681198de0b41f697bd

"Siemens" 800 series 7.3 corrector

TW: “西門子”800系列 7.3校正品
Taiwan flagTaiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Nov 29, 2010 – Nov 29, 2020Cancelled
Registration details
Analysis ID
55c70638948a7e681198de0b41f697bd
Customs Code
DHA00602181700
Company information
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS
Manufacturer Country
United States
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
Used in the "Siemens" 800 series blood gas analysis series, it provides single- and two-point correction of pH and electrolytes and zero correction of carbon monoxide module.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1150 Calibrated Products
Import Information
import
Dates and status
Registration Date
Nov 29, 2010
Expiry Date
Nov 29, 2020
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for "Siemens" 800 series 7.3 corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55c70638948a7e681198de0b41f697bd and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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