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"Tengwang" sterilized sputum pack - Taiwan Registration e257118a5336cc20aa6e9f9abad81c19

Access comprehensive regulatory information for "Tengwang" sterilized 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 e257118a5336cc20aa6e9f9abad81c19 and manufactured by ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Tengwang 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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e257118a5336cc20aa6e9f9abad81c19
Registration Details
Taiwan FDA Registration: e257118a5336cc20aa6e9f9abad81c19
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Device Details

"Tengwang" sterilized sputum pack
TW: "้จฐๆ—บ"ๆป…่ŒๆŠฝ็—ฐๅŒ…
Risk Class 1
Cancelled

Registration Details

e257118a5336cc20aa6e9f9abad81c19

DHA04600039901

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

Input;; Chinese goods

Dates and Status

Jun 29, 2007

Jun 29, 2017

Nov 22, 2019

Cancellation Information

Logged out

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