Pure Global

"Siemens" 800 series 6.838 corrector - Taiwan Registration c5f65dc7098ef68ecf37ae0fa58aef57

Access comprehensive regulatory information for "Siemens" 800 series 6.838 corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5f65dc7098ef68ecf37ae0fa58aef57 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
c5f65dc7098ef68ecf37ae0fa58aef57
Registration Details
Taiwan FDA Registration: c5f65dc7098ef68ecf37ae0fa58aef57
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" 800 series 6.838 corrector
TW: โ€œ่ฅฟ้–€ๅญโ€800็ณปๅˆ—6.838ๆ กๆญฃๅ“
Risk Class 2
Cancelled

Registration Details

c5f65dc7098ef68ecf37ae0fa58aef57

DHA00602155700

Company Information

Product Details

Used in the "Ximenzi" 800 series blood gas analysis series, the slope point is provided as the anometer value and electrolyte correction for the anolyte.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

Input;; Contract manufacturing

Dates and Status

Oct 01, 2010

Oct 01, 2020

May 19, 2022

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ