Taiwan FDA registration a426c4069cd7aea6d52a2fd13e86fb7d

"Xinwei" ENT examination and treatment table (unsterilized)

TW: "新韋" 耳鼻喉檢查及治療檯(未滅菌)

Taiwan·Risk Class 1·SHINWEI INSTRUMENT INDUSTRY LTD.·Registered Nov 10, 2022 – Nov 10, 2027Active

Registration details

Analysis ID: a426c4069cd7aea6d52a2fd13e86fb7d

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 identification range of the "ENT Examination and Treatment Unit (G.5300)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.5300 ENT examination and treatment table
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Nov 10, 2022
Expiry Date: Nov 10, 2027

About this record

Access comprehensive regulatory information for "Xinwei" ENT examination and treatment table (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a426c4069cd7aea6d52a2fd13e86fb7d 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.