Taiwan FDA registration cb81dd0207e912a8a7aaf6d87fe0ae89

"Xinwei" suction tube for otolaryngology (unsterilized)

TW: "新韋" 耳鼻喉科用吸引管 (未滅菌)

Taiwan·Risk Class 1·SHINWEI INSTRUMENT INDUSTRY LTD.·Registered Feb 23, 2023 – Feb 23, 2028Active

Registration details

Analysis ID: cb81dd0207e912a8a7aaf6d87fe0ae89

Company information

Manufacturer: SHINWEI INSTRUMENT INDUSTRY LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHINWEI INSTRUMENT INDUSTRY LTD.

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Feb 23, 2023
Expiry Date: Feb 23, 2028

About this record

Access comprehensive regulatory information for "Xinwei" suction tube for otolaryngology (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb81dd0207e912a8a7aaf6d87fe0ae89 and manufactured by SHINWEI INSTRUMENT INDUSTRY LTD.. The authorized representative in Taiwan is SHINWEI INSTRUMENT INDUSTRY 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.