Taiwan FDA registration ec0633c12b44b5f06c0807848e9dbc0e

"Randox" Lithium 2

TW: "瑞德士"鋰試劑

Taiwan·Risk Class 2·MD·RANDOX LABORATORIES LTD.·Registered May 03, 2019 – May 03, 2024Expired

Registration details

Analysis ID: ec0633c12b44b5f06c0807848e9dbc0e
License Form: Ministry of Health Medical Device Import No. 032419
Customs Code: DHA05603241905

Company information

Manufacturer: RANDOX LABORATORIES LTD.
Manufacturer Country: United Kingdom
Authorized Representative: KUO'S YUAN IN ENTERPRISE CO., LTD.

Product details

Intended Use: This product is used for in vitro diagnostic quantitative determination of lithium in serum. This product is suitable for RX series instruments including RX daytona and RX imola.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A3560 lithium test system
Import Information: Imported from abroad

Dates and status

Registration Date: May 03, 2019
Expiry Date: May 03, 2024

About this record

Access comprehensive regulatory information for "Randox" Lithium 2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec0633c12b44b5f06c0807848e9dbc0e and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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