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"Belia" sputum pack (sterilized) - Taiwan Registration 3d13231549446be9741dabe6b99dbfcd

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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3d13231549446be9741dabe6b99dbfcd
Registration Details
Taiwan FDA Registration: 3d13231549446be9741dabe6b99dbfcd
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Device Details

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

Registration Details

3d13231549446be9741dabe6b99dbfcd

DHA09600196506

Company Information

Product Details

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.

J General hospital and personal use equipment;; D Anesthesiology Science

J.6250 Gloves for patient examination;; D.6810 Tracheobronchial suction tubes

Input;; Chinese goods;; QMS/QSD

Dates and Status

Aug 28, 2013

Aug 28, 2028

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