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"Kaiwei" closed suction sleeve (unsterilized) - Taiwan Registration fa57df1c804b125c3c6ce89f981c4e45

Access comprehensive regulatory information for "Kaiwei" closed suction sleeve (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa57df1c804b125c3c6ce89f981c4e45 and manufactured by KAI WEI (SHENZHEN) CO. LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS 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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fa57df1c804b125c3c6ce89f981c4e45
Registration Details
Taiwan FDA Registration: fa57df1c804b125c3c6ce89f981c4e45
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Device Details

"Kaiwei" closed suction sleeve (unsterilized)
TW: โ€œๆ„ทๅจโ€ๅฏ†้–‰ๅผๆŠฝ็—ฐๅฅ—(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fa57df1c804b125c3c6ce89f981c4e45

DHA04600180109

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

Chinese goods;; input

Dates and Status

Nov 29, 2012

Nov 29, 2022

Apr 12, 2024

Cancellation Information

Logged out

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