Taiwan FDA registration f37545f73f30dc80d64eac990d210898

"Randox" Ammonia (NH3) (Non-Sterile)

TW: "瑞德士" 血氨試劑 (未滅菌)

Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LTD.·Registered Aug 02, 2018 – Aug 02, 2023Expired

Registration details

Analysis ID: f37545f73f30dc80d64eac990d210898
License Form: Ministry of Health Medical Device Import No. 019439
Customs Code: DHA09401943902

Company information

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

Product details

Intended Use: Limited to the first level identification range of the blood ammonia test system (A.1065) of the management method for medical equipment.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1065 Blood Ammonia Test System
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 02, 2018
Expiry Date: Aug 02, 2023

About this record

Access comprehensive regulatory information for "Randox" Ammonia (NH3) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f37545f73f30dc80d64eac990d210898 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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