Taiwan FDA registration c0396e18f72bd63ee48a5af37651d41c

"Hejie" sputum pack (sterilization)

TW: "禾捷"抽痰包(滅菌)

Taiwan·Risk Class 1·Zhangjiagang Huaxing Rubber-Plastic Products Co., Ltd.·Registered Jan 08, 2018 – Jan 08, 2028Active

Registration details

Analysis ID: c0396e18f72bd63ee48a5af37651d41c
Customs Code: DHA09600331605

Company information

Manufacturer: Zhangjiagang Huaxing Rubber-Plastic Products Co., Ltd.
Manufacturer Country: China
Authorized Representative: HE JIE Medical Products Co., Ltd.

Product details

Intended Use: It is limited to the first level of identification of the "Tracheobronchial Suction Catheter (D.6810)" and "Gloves for Patient Examination (J.6250)" of 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: Input;; Chinese goods

Dates and status

Registration Date: Jan 08, 2018
Expiry Date: Jan 08, 2028

About this record

Access comprehensive regulatory information for "Hejie" sputum pack (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0396e18f72bd63ee48a5af37651d41c and manufactured by Zhangjiagang Huaxing Rubber-Plastic Products Co., Ltd.. The authorized representative in Taiwan is HE JIE Medical Products Co., Ltd..

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