Taiwan FDA registration 5d7a510f99ccb5369d4139b9bfd4db6d

Canon electrolyte reference solution

TW: 佳能電解質參考溶液
Taiwan flagTaiwan·Risk Class 2·CANON MEDICAL SYSTEMS CORPORATION·Registered Oct 27, 2022 – Oct 27, 2027Active
Registration details
Analysis ID
5d7a510f99ccb5369d4139b9bfd4db6d
Customs Code
DHA05603587102
Company information
Manufacturer Country
Japan
Authorized Representative
TUNYEN ENTERPRISE CORPORATION
Product details
Intended Use
This product is used as a reference solution for the ion-selective electrode equipped with Canon's automated biochemical analysis instrument (model: TBA-nx360) for the determination of electrolyte concentration (Na+, K+, C1-) in serum or urine.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1170 氯化物試驗系統;; A.1665 鈉試驗系統;; A.1600 鉀試驗系統
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 27, 2022
Expiry Date
Oct 27, 2027
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About this record

Access comprehensive regulatory information for Canon electrolyte reference solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5d7a510f99ccb5369d4139b9bfd4db6d and manufactured by CANON MEDICAL SYSTEMS CORPORATION. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DENKA CO., LTD, and 1 recent registrations in the same category. 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.

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