Taiwan FDA registration 4bec7f715364c8b37769433e82266be5

"Ai Xi Fu" Suction Pack (Sterilized)

TW: "愛僖福" 抽痰包 (滅菌)

Taiwan·Risk Class 1·Zhangjiagang Huaxing Rubber-Plastic Products Co., Ltd.·Registered Jun 18, 2024 – Jun 18, 2029Active

Registration details

Analysis ID: 4bec7f715364c8b37769433e82266be5
Customs Code: DHA09600495505

Company information

Manufacturer: Zhangjiagang Huaxing Rubber-Plastic Products Co., Ltd.
Manufacturer Country: China
Authorized Representative: MEDIFLY CO., LTD.

Product details

Intended Use: It is limited to the first level of identification of "tracheobronchial suction catheter (D.6810)" and "gloves for patient examination (J.6250)" in the classification and grading management measures for medical devices.
Product Type (Level 1): J General hospital and personal use equipment;; D Anesthesiology Science
Product Type (Level 2): J.6250 Gloves for patient examination;; D.6810 Tracheobronchial suction tubes
Import Information: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: Jun 18, 2024
Expiry Date: Jun 18, 2029

About this record

Access comprehensive regulatory information for "Ai Xi Fu" Suction Pack (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4bec7f715364c8b37769433e82266be5 and manufactured by Zhangjiagang Huaxing Rubber-Plastic Products Co., Ltd.. The authorized representative in Taiwan is MEDIFLY CO., LTD..

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