Taiwan FDA registration 2b06a74b3ee351bcb1c218baddb2b826

“Headstar” Handhold Suction Unit (Non-sterile)

TW: “華德” 手動式抽吸器(未滅菌)

Taiwan·Risk Class 1·MD·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered Aug 22, 2018 – Aug 22, 2028Active

Registration details

Analysis ID: 2b06a74b3ee351bcb1c218baddb2b826
License Form: Ministry of Health Medical Device Manufacturing No. 007396

Company information

Manufacturer: HEADSTAR MEDICAL PRODUCTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HEADSTAR MEDICAL PRODUCTS 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 and plastic surgical devices
Product Type (Level 2): I4680 Non-powered, single-patient, portable suction device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 22, 2018
Expiry Date: Aug 22, 2028

About this record

Access comprehensive regulatory information for “Headstar” Handhold Suction Unit (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2b06a74b3ee351bcb1c218baddb2b826 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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