Taiwan FDA registration e1c6ee06f595ae671a48e439e4a7da84

"Nova" Uric acid control solution(Non-Sterile)

TW: "露華" 尿酸品管液 (未滅菌)

Taiwan·Risk Class 1·MD·NOVA BIOMEDICAL CORPORATION·Registered Mar 02, 2018 – Mar 02, 2023Expired

Registration details

Analysis ID: e1c6ee06f595ae671a48e439e4a7da84
License Form: Ministry of Health Medical Device Import No. 018854
Customs Code: DHA09401885409

Company information

Manufacturer: NOVA BIOMEDICAL CORPORATION
Manufacturer Country: United States
Authorized Representative: NOVA BIOMEDICAL TAIWAN CORP.

Product details

Intended Use: Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information: Imported from abroad

Dates and status

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

About this record

Access comprehensive regulatory information for "Nova" Uric acid control solution(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 e1c6ee06f595ae671a48e439e4a7da84 and manufactured by NOVA BIOMEDICAL CORPORATION. The authorized representative in Taiwan is NOVA BIOMEDICAL TAIWAN CORP..

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