Taiwan FDA registration 12409d4150fd127fff7608e46e0a3fd7

"Wandong" magnetic resonance imaging system

TW: “萬東”磁振造影系統
Taiwan flagTaiwan·Risk Class 2·Beijing Wandong Medical Technology Co., Ltd.·Registered Mar 17, 2022 – Mar 17, 2027Active
Registration details
Analysis ID
12409d4150fd127fff7608e46e0a3fd7
Customs Code
DHA09200132503
Company information
Manufacturer Country
China
Authorized Representative
DERMACARE BIOMED INC.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1000 磁振診斷裝置
Import Information
The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". Input;; Chinese goods
Dates and status
Registration Date
Mar 17, 2022
Expiry Date
Mar 17, 2027
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About this record

Access comprehensive regulatory information for "Wandong" magnetic resonance imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12409d4150fd127fff7608e46e0a3fd7 and manufactured by Beijing Wandong Medical Technology Co., Ltd.. The authorized representative in Taiwan is DERMACARE BIOMED INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Beijing Wandong Medical Technology Co., Ltd., 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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