Taiwan FDA registration 48e025b6b66e6c337ea3488fb455fca8

"Ryan" Thesia arthroscopic surgical system

TW: “瑞安”泰西亞關節鏡手術系統
Taiwan flagTaiwan·Risk Class 2·Peter's Technology (Suzhou) Co., Ltd;; RELIGN Corporation·Registered May 28, 2024 – May 28, 2029Active
Registration details
Analysis ID
48e025b6b66e6c337ea3488fb455fca8
Customs Code
DHA09200156204
Company information
Manufacturer Country
United States;;China
Authorized Representative
ZIMMER BIOMET TAIWAN CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
N Orthopedics;; I General, Plastic Surgery and Dermatology
Product Type (Level 2)
N.1100 Closing Lenses;; I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information
Contract manufacturing;; Chinese goods;; input
Dates and status
Registration Date
May 28, 2024
Expiry Date
May 28, 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 48e025b6b66e6c337ea3488fb455fca8 and manufactured by Peter's Technology (Suzhou) Co., Ltd;; 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 AB Medical Technologies, Inc.;; 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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