Taiwan FDA registration 82e0e1ebaba40f06998271fd82d7a791

"Pacific" high flow rate suction flush kit

TW: “太平洋”高流速抽吸沖洗套組

Taiwan·Risk Class 2·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Apr 20, 2021 – Apr 20, 2026Expired

Registration details

Analysis ID: 82e0e1ebaba40f06998271fd82d7a791

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: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: Domestic

Dates and status

Registration Date: Apr 20, 2021
Expiry Date: Apr 20, 2026

About this record

Access comprehensive regulatory information for "Pacific" high flow rate suction flush kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82e0e1ebaba40f06998271fd82d7a791 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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