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"Qinda" suction tube (sterilized) - Taiwan Registration fdd9fa01a0e7d2cc81ec3eb3ea74aafb

Access comprehensive regulatory information for "Qinda" suction tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fdd9fa01a0e7d2cc81ec3eb3ea74aafb and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT 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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fdd9fa01a0e7d2cc81ec3eb3ea74aafb
Registration Details
Taiwan FDA Registration: fdd9fa01a0e7d2cc81ec3eb3ea74aafb
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Device Details

"Qinda" suction tube (sterilized)
TW: โ€œๅ‹ค้”โ€ๆŠฝ็—ฐ็ฎก๏ผˆๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

fdd9fa01a0e7d2cc81ec3eb3ea74aafb

DHA04400578005

Company Information

Product Details

Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Apr 20, 2007

Apr 20, 2022

Apr 12, 2024

Cancellation Information

Logged out

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