Taiwan FDA registration ec56c3abaea4a5393162f460c41fb260

Badiek Rotavirus/Adenovirus Test Reagent - Tube Solution

TW: 巴迪鐵克輪狀病毒/腺病毒檢驗試劑-品管液

Taiwan·Risk Class 2·Boditech Med Inc.·Registered Nov 02, 2022 – Nov 02, 2027Active

Registration details

Analysis ID: ec56c3abaea4a5393162f460c41fb260
Customs Code: DHA05603587701

Company information

Manufacturer: Boditech Med Inc.
Manufacturer Country: Korea, Republic of
Authorized Representative: MEDRICH INSTRUMENT CO., LTD.

Product details

Intended Use: This product is used for quality management of rotavirus/adenovirus testing reagents manufactured by Boditech Med Inc. for in vitro diagnostic purposes.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Quality control materials (analytical and non-analytical)
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Nov 02, 2022
Expiry Date: Nov 02, 2027

About this record

Access comprehensive regulatory information for Badiek Rotavirus/Adenovirus Test Reagent - Tube Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec56c3abaea4a5393162f460c41fb260 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

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