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"Belia" sputum pack (sterilized) - Taiwan Registration e83d596c7d1acd46872830510ddcd1ef

Access comprehensive regulatory information for "Belia" sputum pack (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e83d596c7d1acd46872830510ddcd1ef 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, 1 companies making similar products including JIANGSU YAOHUA MEDICAL DEVICE TECHNOLOGY CO., LTD, and 1 recent registrations in the same category. 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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e83d596c7d1acd46872830510ddcd1ef
Registration Details
Taiwan FDA Registration: e83d596c7d1acd46872830510ddcd1ef
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Device Details

"Belia" sputum pack (sterilized)
TW: โ€œ่““่މ้›…โ€ๆŠฝ็—ฐๅŒ… (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e83d596c7d1acd46872830510ddcd1ef

DHA04600043607

Company Information

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Tracheobronchial Suction Catheter (D.6810) and Gloves for Patient Examination (J.6250)".

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

Chinese goods;; Input;; QMS/QSD

Dates and Status

Oct 23, 2007

Oct 23, 2012

Mar 27, 2014

Cancellation Information

Logged out

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