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"Headstar" Reservoir Bag (Non-sterile) - Taiwan Registration 8cf600252cdc6c33ac85b5a59f1505b2

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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8cf600252cdc6c33ac85b5a59f1505b2
Registration Details
Taiwan FDA Registration: 8cf600252cdc6c33ac85b5a59f1505b2
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Device Details

"Headstar" Reservoir Bag (Non-sterile)
TW: "่ฏๅพท" ๅ„ฒๆฐฃๅ›Š (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8cf600252cdc6c33ac85b5a59f1505b2

Ministry of Health Medical Device Manufacturing No. 007257

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the "Air Storage Bag (D.5320)" of the Measures for the Administration of Medical Equipment.

D Devices for anesthesiology

D5320 air reservoir

Produced in Taiwan, China

Dates and Status

May 14, 2018

May 14, 2028