Taiwan FDA registration a520f7b6a427b1227b8a87cd9c3e8225
"Rongfeng" Manual Orthopedic Surgical Instruments (Unsterilized)
TW: "榮楓" 手動式骨科手術器械 (未滅菌)
Registration details
- Analysis ID
- a520f7b6a427b1227b8a87cd9c3e8225
Company information
- Manufacturer
- DIGITAL-CAN TECH. CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- G-Maple Technology Co., Ltd.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Sep 03, 2020
- Expiry Date
- Sep 03, 2025
About this record
Access comprehensive regulatory information for "Rongfeng" Manual Orthopedic Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a520f7b6a427b1227b8a87cd9c3e8225 and manufactured by DIGITAL-CAN TECH. CO., LTD.. The authorized representative in Taiwan is G-Maple Technology 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