Taiwan FDA registration 2621637c2691ec4b8a0e9188dc5fa83f

"Ryan" Thesia arthroscopic surgical system

TW: “瑞安”泰西亞關節鏡手術系統
Taiwan flagTaiwan·Risk Class 2·AB Medical Technologies, Inc.;; RELIGN Corporation·Registered May 15, 2024 – May 15, 2029Active
Registration details
Analysis ID
2621637c2691ec4b8a0e9188dc5fa83f
Customs Code
DHA05603717107
Company information
Manufacturer Country
United States
Authorized Representative
ZIMMER BIOMET TAIWAN CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
May 15, 2024
Expiry Date
May 15, 2029
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About this record

Access comprehensive regulatory information for "Ryan" Thesia arthroscopic surgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2621637c2691ec4b8a0e9188dc5fa83f and manufactured by AB Medical Technologies, Inc.;; RELIGN Corporation. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Peter's Technology (Suzhou) Co., Ltd;; RELIGN Corporation, and 1 recent registrations in the same category. 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.

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