Taiwan FDA registration 2d8327c6f6acf8a443e75ac715923285

"Prowei" chest drainage bottle (sterilized)

TW: "普威" 胸腔引流瓶 (滅菌)

Taiwan·Risk Class 1·Puwei International Co., Ltd. Yilan Factory·Registered Dec 21, 2016 – Dec 21, 2026Active

Registration details

Analysis ID: 2d8327c6f6acf8a443e75ac715923285

Company information

Manufacturer: Puwei International Co., Ltd. Yilan Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: UNIMAX MEDICAL SYSTEMS INC.

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Dec 21, 2016
Expiry Date: Dec 21, 2026

About this record

Access comprehensive regulatory information for "Prowei" chest drainage bottle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d8327c6f6acf8a443e75ac715923285 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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