Taiwan FDA registration d672720273f1253c31984bbd4f6b8dd6

Sejizu Snassi leap uric acid standard

TW: 積水思納西閏尿酸標準液

Taiwan·Risk Class 2·SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT·Registered Dec 15, 2005 – Dec 15, 2025Expired

Registration details

Analysis ID: d672720273f1253c31984bbd4f6b8dd6
Customs Code: DHA00601558506

Company information

Manufacturer: SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT
Manufacturer Country: Japan
Authorized Representative: KUO'S YUAN IN ENTERPRISE CO., LTD.

Product details

Intended Use: It is used as a correction solution for the determination of uric acid concentration in human serum or urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: import

Dates and status

Registration Date: Dec 15, 2005
Expiry Date: Dec 15, 2025

About this record

Access comprehensive regulatory information for Sejizu Snassi leap uric acid standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d672720273f1253c31984bbd4f6b8dd6 and manufactured by SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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