Taiwan FDA registration 55f6b6cdbe441dff06d05fa66ad46c90

"Pacific" extraction apparatus (sterile)

TW: “太平洋”抽吸器具 (滅菌)

Taiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Mar 07, 2014 – Mar 07, 2029Active

Registration details

Analysis ID: 55f6b6cdbe441dff06d05fa66ad46c90

Company information

Manufacturer: Pacific Medical Materials Co., Ltd. Copper Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PACIFIC HOSPITAL SUPPLY CO., LTD.

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: 國產;; QMS/QSD

Dates and status

Registration Date: Mar 07, 2014
Expiry Date: Mar 07, 2029

About this record

Access comprehensive regulatory information for "Pacific" extraction apparatus (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55f6b6cdbe441dff06d05fa66ad46c90 and manufactured by Pacific Medical Materials Co., Ltd. Copper Factory. The authorized representative in Taiwan is PACIFIC HOSPITAL SUPPLY CO., LTD..

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