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"Jiahong" drip rack (unsterilized) - Taiwan Registration 9d47c83b9c6b6b1e36ef7944c836e2ed

Access comprehensive regulatory information for "Jiahong" drip rack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d47c83b9c6b6b1e36ef7944c836e2ed and manufactured by JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY 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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9d47c83b9c6b6b1e36ef7944c836e2ed
Registration Details
Taiwan FDA Registration: 9d47c83b9c6b6b1e36ef7944c836e2ed
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Device Details

"Jiahong" drip rack (unsterilized)
TW: โ€œไฝณ้ดปโ€้ปžๆปดๆžถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9d47c83b9c6b6b1e36ef7944c836e2ed

DHA04600059300

Product Details

Limited to the first level identification range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.

J General hospital and personal use equipment

J.6990 Injection holder

Input;; Chinese goods

Dates and Status

Nov 12, 2008

Nov 12, 2023