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“Headstar” Anesthesia Breathing Circuit (Non-sterile) - Taiwan Registration e0b53d9c1243d6e2d0c9a05a02094fbb

Access comprehensive regulatory information for “Headstar” Anesthesia Breathing Circuit (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 e0b53d9c1243d6e2d0c9a05a02094fbb and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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e0b53d9c1243d6e2d0c9a05a02094fbb
Registration Details
Taiwan FDA Registration: e0b53d9c1243d6e2d0c9a05a02094fbb
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Device Details

“Headstar” Anesthesia Breathing Circuit (Non-sterile)
TW: “華德”麻醉呼吸管路(未滅菌)
Risk Class 1
MD

Registration Details

e0b53d9c1243d6e2d0c9a05a02094fbb

Ministry of Health Medical Device Manufacturing No. 007633

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "anesthesia breathing circuit (D.5240)" of the Measures for the Administration of Medical Equipment.

D Devices for anesthesiology

D5240 Anesthesia breathing line

Produced in Taiwan, China

Dates and Status

Jan 24, 2019

Jan 24, 2024