Taiwan FDA registration 153f926a713e4ece0831faee184af6ad

"Nippon Optoelectronics" automatic blood and red blood cell sedimentation rate analyzer

TW: "日本光電" 全自動血液及紅血球沉降速率分析儀

Taiwan·Risk Class 2·NIHON PER TOMIOKA CORPORATION;; NIHON PER CORPORATION·Registered Oct 03, 2022 – Oct 03, 2027Active

Registration details

Analysis ID: 153f926a713e4ece0831faee184af6ad
Customs Code: DHA05603586109

Company information

Manufacturer: NIHON PER TOMIOKA CORPORATION;; NIHON PER CORPORATION
Manufacturer Country: Japan
Authorized Representative: K&C MEDICAL CO., LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.5800 Automatic sedimentation rate device;; B.5220 Automatic Differentiation Cell Counter
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Oct 03, 2022
Expiry Date: Oct 03, 2027

About this record

Access comprehensive regulatory information for "Nippon Optoelectronics" automatic blood and red blood cell sedimentation rate analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 153f926a713e4ece0831faee184af6ad and manufactured by NIHON PER TOMIOKA CORPORATION;; NIHON PER CORPORATION. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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