Taiwan FDA registration ba39da58dbdb2ca82622536bd3b37480

Innova RNP chemical cold light immunoassay correction solution

TW: 因諾瓦RNP化學冷光免疫分析法校正液

Taiwan·Risk Class 2·INOVA DIAGNOSTICS, INC.·Registered Feb 12, 2015 – Feb 12, 2030Active

Registration details

Analysis ID: ba39da58dbdb2ca82622536bd3b37480
Customs Code: DHA05602707403

Company information

Manufacturer: INOVA DIAGNOSTICS, INC.
Manufacturer Country: United States
Authorized Representative: TRUGENE DIAGNOSTICS, INC.

Product details

Intended Use: This product establishes the reference point of the working curve so that the unit value can be calculated for the detection of RNP immunoglobulin G antibody in human serological samples by QUANTA Flash RNP chemical cold light immunoassay.
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: Feb 12, 2015
Expiry Date: Feb 12, 2030

About this record

Access comprehensive regulatory information for Innova RNP chemical cold light immunoassay correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba39da58dbdb2ca82622536bd3b37480 and manufactured by INOVA DIAGNOSTICS, INC.. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..

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