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Tengwang sputum pack - Taiwan Registration 9a11cdbfe5064dc57622e0e0f19ebf3b

Access comprehensive regulatory information for Tengwang sputum pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a11cdbfe5064dc57622e0e0f19ebf3b and manufactured by ZHANGJIAGANG WENHAO INDUSTRY CO., LTD.. The authorized representative in Taiwan is LUXVIEW INTERNATIONAL 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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9a11cdbfe5064dc57622e0e0f19ebf3b
Registration Details
Taiwan FDA Registration: 9a11cdbfe5064dc57622e0e0f19ebf3b
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Device Details

Tengwang sputum pack
TW: ้จฐๆ—บๆŠฝ็—ฐๅŒ…
Risk Class 1
Cancelled

Registration Details

9a11cdbfe5064dc57622e0e0f19ebf3b

DHA04600006702

Company Information

Product Details

The bronchial bronchial suction guide is a device used to extract liquids or semi-solids from the patient's upper airway.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

Chinese goods;; input

Dates and Status

Nov 29, 2005

Nov 29, 2010

Nov 30, 2012

Cancellation Information

Logged out

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