Taiwan FDA registration 233fedf037d724e06ba868188101d4a1

Roche Blood Gas Electrolyte Analyzer Cobas B 221

TW: 羅氏血液氣體電解質分析儀 cobas b 221
Taiwan flagTaiwan·Risk Class 2·Roche Diagnostics International Ltd;; ROCHE DIAGNOSTICS GMBH·Registered Mar 08, 2006 – Mar 08, 2026Expired
Registration details
Analysis ID
233fedf037d724e06ba868188101d4a1
Customs Code
DHA00601611602
Company information
Manufacturer Country
Germany;;Switzerland
Authorized Representative
ROCHE DIAGNOSTICS LTD.
Product details
Intended Use
The Roche Blood Gas Omni S is a modular analyzer that measures blood gas, electrolytes, total heme, oxygen saturation and blood cell volume ratio from whole blood, serum, plasma, acetic acid and bicarbonate including dialysate and QC materials.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1120 血內氣體(PCO2,PO2)及血液pH值試驗系統
Import Information
import
Dates and status
Registration Date
Mar 08, 2006
Expiry Date
Mar 08, 2026
About this record

Access comprehensive regulatory information for Roche Blood Gas Electrolyte Analyzer Cobas B 221 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 233fedf037d724e06ba868188101d4a1 and manufactured by Roche Diagnostics International Ltd;; ROCHE DIAGNOSTICS GMBH. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..

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