Taiwan FDA registration 968a134dd79ca011b00dd245ff803487

Japanese photoelectric blood analyzer

TW: 日本光電血液分析儀
Taiwan flagTaiwan·Risk Class 2·NIHON KOHDEN CORPORATION·Registered Jan 03, 2007 – Jan 03, 2012Cancelled
Registration details
Analysis ID
968a134dd79ca011b00dd245ff803487
Customs Code
DHA00601785901
Company information
Manufacturer Country
Japan
Authorized Representative
Jingxiang Co., Ltd
Product details
Intended Use
Hematology analyzer MEK-6318、6400 J 是設計來同時測量血液中18項參數.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.5200 Automated Cell Counter
Import Information
import
Dates and status
Registration Date
Jan 03, 2007
Expiry Date
Jan 03, 2012
Cancellation Date
May 05, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Japanese photoelectric blood analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 968a134dd79ca011b00dd245ff803487 and manufactured by NIHON KOHDEN CORPORATION. The authorized representative in Taiwan is Jingxiang Co., 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