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"HSINER" Reservoir bag (Non-sterile) - Taiwan Registration 89e1bb94fbde2af4aaed3e13829a77a7

Access comprehensive regulatory information for "HSINER" 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 89e1bb94fbde2af4aaed3e13829a77a7 and manufactured by ML PRODUCTS, L.L.C.. The authorized representative in Taiwan is HSINER 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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89e1bb94fbde2af4aaed3e13829a77a7
Registration Details
Taiwan FDA Registration: 89e1bb94fbde2af4aaed3e13829a77a7
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Device Details

"HSINER" Reservoir bag (Non-sterile)
TW: "ๆ–ฐๅปฃๆฅญ" ๅ„ฒๆฐฃๅ›Š(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

89e1bb94fbde2af4aaed3e13829a77a7

Ministry of Health Medical Device Import No. 014371

DHA09401437108

Company Information

United States

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

Imported from abroad

Dates and Status

Jul 28, 2014

Jul 28, 2024