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"Dicheng" pressure line and its accessories (unsterilized) - Taiwan Registration 380d0e3b3da9f7fae5f3e298bacbe594

Access comprehensive regulatory information for "Dicheng" pressure line and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 380d0e3b3da9f7fae5f3e298bacbe594 and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..

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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380d0e3b3da9f7fae5f3e298bacbe594
Registration Details
Taiwan FDA Registration: 380d0e3b3da9f7fae5f3e298bacbe594
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Device Details

"Dicheng" pressure line and its accessories (unsterilized)
TW: โ€œ็‹„ๆˆโ€ๅฃ“ๅŠ›็ฎก่ทฏๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

380d0e3b3da9f7fae5f3e298bacbe594

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of pressure pipelines and their accessories (D.5860) of the classification and grading management measures for medical devices.

D Anesthesiology

D.5860 Pressure lines and accessories thereof

Domestic

Dates and Status

Apr 06, 2009

Apr 06, 2024