Taiwan FDA registration 8cf600252cdc6c33ac85b5a59f1505b2

"Headstar" Reservoir Bag (Non-sterile)

TW: "華德" 儲氣囊 (未滅菌)

Taiwan·Risk Class 1·MD·HEADSTAR MEDICAL PRODUCTS CO., LTD.·Registered May 14, 2018 – May 14, 2028Active

Registration details

Analysis ID: 8cf600252cdc6c33ac85b5a59f1505b2
License Form: Ministry of Health Medical Device Manufacturing No. 007257

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 identification scope of the "Air Storage Bag (D.5320)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5320 air reservoir
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 14, 2018
Expiry Date: May 14, 2028

About this record

Access comprehensive regulatory information for "Headstar" Reservoir Bag (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 8cf600252cdc6c33ac85b5a59f1505b2 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS CO., LTD..

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