Taiwan FDA registration 9b3f1c9df3f40e9febf0cd57ed2925da
"Shengmai" Le Cordon Bleu rib fixation system
TW: “生邁”藍帶肋骨固定系統
Taiwan·Risk Class 2·BIOMET ORTHOPEDICS;; BIOMET Microfixation·Registered Sep 06, 2017 – Sep 06, 2022CancelledRegistration details
- Analysis ID
- 9b3f1c9df3f40e9febf0cd57ed2925da
- Customs Code
- DHA05603021202
Company information
- Manufacturer
- BIOMET ORTHOPEDICS;; BIOMET Microfixation
- Manufacturer Country
- United States
- Authorized Representative
- Yangzhi Biotechnology Co., Ltd
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.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Sep 06, 2017
- Expiry Date
- Sep 06, 2022
- Cancellation Date
- Mar 06, 2024
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Shengmai" Le Cordon Bleu rib fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9b3f1c9df3f40e9febf0cd57ed2925da and manufactured by BIOMET ORTHOPEDICS;; BIOMET Microfixation. The authorized representative in Taiwan is Yangzhi Biotechnology Co., 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.
Free DatabasePowered by Pure Global AI89,000+ Devices