Taiwan FDA registration 96d953922ec4eb9c38b92a413b8361ca
"Xiangyuan" nasal fixation splint (sterilization)
TW: "翔源"鼻腔內固定夾板(滅菌)
Registration details
- Analysis ID
- 96d953922ec4eb9c38b92a413b8361ca
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MEDFRONT MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of "Intranasal Splint (G.4780)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4780 Nasal fixations
- Import Information
- 國產;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Sep 09, 2014
- Expiry Date
- Sep 09, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Xiangyuan" nasal fixation splint (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 96d953922ec4eb9c38b92a413b8361ca and manufactured by Hekang Biotechnology Co., Ltd. Biomedical Products Factory. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices