Taiwan FDA registration 3b913f36f2d337b70bbe616f4d0ceb68

"Practical" Zhang's stirred fecal collection bottle (unsterilized)

TW: "實用" 張氏攪拌型糞便收集瓶(未滅菌)

Taiwan·Risk Class 1·SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.·Registered Dec 28, 2022 – Dec 28, 2027Active

Registration details

Analysis ID: 3b913f36f2d337b70bbe616f4d0ceb68

Company information

Manufacturer: SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2900 Microbial sample collection and delivery equipment
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Dec 28, 2022
Expiry Date: Dec 28, 2027

About this record

Access comprehensive regulatory information for "Practical" Zhang's stirred fecal collection bottle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3b913f36f2d337b70bbe616f4d0ceb68 and manufactured by SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD..

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