Taiwan FDA registration f55e4adb33c4b65824e06e5e0ee4b552

“Nihon Kohden” Automated Hematology Analyzer Celltac α

TW: “日本光電” 自動血液分析儀

Taiwan·Risk Class 2·MD·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Aug 08, 2018 – Aug 08, 2023Expired

Registration details

Analysis ID: f55e4adb33c4b65824e06e5e0ee4b552
License Form: Ministry of Health Medical Device Import No. 031406
Customs Code: DHA05603140604

Company information

Manufacturer: Nihon Kohden Tomioka Corporation Tomioka Production Center
Manufacturer Country: Japan
Authorized Representative: K&C MEDICAL CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B5200 Automated Cell Counter
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 08, 2018
Expiry Date: Aug 08, 2023

About this record

Access comprehensive regulatory information for “Nihon Kohden” Automated Hematology Analyzer Celltac α in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f55e4adb33c4b65824e06e5e0ee4b552 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The authorized representative in Taiwan is K&C MEDICAL 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.