Taiwan FDA registration 1b36c5f64d9b5bfffe84965a8168ac5f

"Shinjun" manual drawer (not sterilized)

TW: "新駿" 手動式抽吸器 (未滅菌)

Taiwan·Risk Class 1·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered May 22, 2017 – May 22, 2022Cancelled

Registration details

Analysis ID: 1b36c5f64d9b5bfffe84965a8168ac5f

Company information

Manufacturer: HEADSTAR MEDICAL PRODUCTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: STURDY INDUSTRIAL CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4680 Non-motive, single patient-use, carry-on suctioning device
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: May 22, 2017
Expiry Date: May 22, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Shinjun" manual drawer (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b36c5f64d9b5bfffe84965a8168ac5f and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is STURDY INDUSTRIAL CO., LTD..

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