"Wandong" magnetic resonance imaging system
- Analysis ID
- 12409d4150fd127fff7608e46e0a3fd7
- Customs Code
- DHA09200132503
- Manufacturer
- Beijing Wandong Medical Technology Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- DERMACARE BIOMED INC.
- 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
- Registration Date
- Mar 17, 2022
- Expiry Date
- Mar 17, 2027
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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.