Taiwan FDA registration e83d596c7d1acd46872830510ddcd1ef

"Belia" sputum pack (sterilized)

TW: “蓓莉雅”抽痰包 (滅菌)
Taiwan flagTaiwan·Risk Class 1·ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.·Registered Oct 23, 2007 – Oct 23, 2012Cancelled
Registration details
Analysis ID
e83d596c7d1acd46872830510ddcd1ef
Customs Code
DHA04600043607
Company information
Manufacturer Country
China
Authorized Representative
Tengwang Co., Ltd
Product details
Intended Use
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)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.6810 Pneumatic bronchial suction guide tube
Import Information
Chinese goods;; Input;; QMS/QSD
Dates and status
Registration Date
Oct 23, 2007
Expiry Date
Oct 23, 2012
Cancellation Date
Mar 27, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

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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