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“Headstar” Nebulizer Kit and Accessory - Taiwan Registration fc6121901afe7e843d791698c5c6b328

Access comprehensive regulatory information for “Headstar” Nebulizer Kit and Accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc6121901afe7e843d791698c5c6b328 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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fc6121901afe7e843d791698c5c6b328
Registration Details
Taiwan FDA Registration: fc6121901afe7e843d791698c5c6b328
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Device Details

“Headstar” Nebulizer Kit and Accessory
TW: “華德”噴霧罐組及配件
Risk Class 2
MD

Registration Details

fc6121901afe7e843d791698c5c6b328

Ministry of Health Medical Device Manufacturing No. 005970

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5630 Sprayer

Produced in Taiwan, China

Dates and Status

Jan 13, 2018

Jan 13, 2028