Taiwan FDA registration 3d13231549446be9741dabe6b99dbfcd

"Belia" sputum pack (sterilized)

TW: “蓓莉雅”抽痰包 (滅菌)
Taiwan flagTaiwan·Risk Class 1·JIANGSU YAOHUA MEDICAL DEVICE TECHNOLOGY CO., LTD·Registered Aug 28, 2013 – Aug 28, 2028Active
Registration details
Analysis ID
3d13231549446be9741dabe6b99dbfcd
Customs Code
DHA09600196506
Company information
Manufacturer Country
China
Authorized Representative
BELIA CORPORATION
Product details
Intended Use
It is limited to the first level of identification of the "Tracheobronchial Suction Catheter (D.6810)" and "Gloves for Patient Examination (J.6250)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1)
J General hospital and personal use equipment;; D Anesthesiology Science
Product Type (Level 2)
J.6250 Gloves for patient examination;; D.6810 Tracheobronchial suction tubes
Import Information
Input;; Chinese goods;; QMS/QSD
Dates and status
Registration Date
Aug 28, 2013
Expiry Date
Aug 28, 2028
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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 3d13231549446be9741dabe6b99dbfcd and manufactured by JIANGSU YAOHUA MEDICAL DEVICE TECHNOLOGY CO., LTD. The authorized representative in Taiwan is BELIA CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS 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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