Taiwan FDA registration 23b77b03861c5036aeba62f06f0e0b84

"Euro Fest" manual spine surgical instruments (unsterilized)

TW: “歐御費絲特” 脊椎手動式手術器械(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Royal Medical Equipment Industry Co., Ltd.;; Proteex Biotech Co., Ltd·Registered Jul 04, 2019 – Jul 04, 2029Active
Registration details
Analysis ID
23b77b03861c5036aeba62f06f0e0b84
Company information
Manufacturer Country
Taiwan, Province of China
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
國產;; QMS/QSD;; 委託製造
Dates and status
Registration Date
Jul 04, 2019
Expiry Date
Jul 04, 2029
About this record

Access comprehensive regulatory information for "Euro Fest" manual spine 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 23b77b03861c5036aeba62f06f0e0b84 and manufactured by Royal Medical Equipment Industry Co., Ltd.;; Proteex Biotech Co., Ltd. The authorized representative in Taiwan is EUROPE ROYAL MEDICAL DEVICES INDUSTRIAL 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