Taiwan FDA registration b71c923428cb27f0a1c6d9d8f47f22aa

"Changmei Medical" vertebral body dilation balloon catheter (unsterilized)

TW: “常美醫療”椎體擴張球囊導管(未滅菌)

Taiwan·Risk Class 2·中央醫療器材股份有限公司;; Jiangsu Changmei Medtech Co., Ltd.·Registered Jan 12, 2017 – Jan 12, 2027Active

Registration details

Analysis ID: b71c923428cb27f0a1c6d9d8f47f22aa
Customs Code: DHA09200079509

Company information

Manufacturer: 中央醫療器材股份有限公司;; Jiangsu Changmei Medtech Co., Ltd.
Manufacturer Country: Taiwan, Province of China;;China
Authorized Representative: CENTRAL MEDICAL TECHNOLOGIES INC.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.9999 Miscellaneous
Import Information: Contract manufacturing;; Chinese goods;; input

Dates and status

Registration Date: Jan 12, 2017
Expiry Date: Jan 12, 2027

About this record

Access comprehensive regulatory information for "Changmei Medical" vertebral body dilation balloon catheter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b71c923428cb27f0a1c6d9d8f47f22aa and manufactured by 中央醫療器材股份有限公司;; Jiangsu Changmei Medtech Co., Ltd.. The authorized representative in Taiwan is CENTRAL MEDICAL TECHNOLOGIES INC..

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.