Taiwan FDA registration 27a37206f2c1df281a7f7e665be4bd0a

"Philips" magnetic resonance imaging system

TW: “飛利浦”磁振造影系統
Taiwan flagTaiwan·Risk Class 2·Philips Healthcare (Suzhou) Co., Ltd·Registered Apr 11, 2022 – Apr 11, 2027Active
Registration details
Analysis ID
27a37206f2c1df281a7f7e665be4bd0a
Customs Code
DHA09200132707
Company information
Manufacturer Country
China
Authorized Representative
PHILIPS TAIWAN LIMITED
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
Input;; 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.
Dates and status
Registration Date
Apr 11, 2022
Expiry Date
Apr 11, 2027
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About this record

Access comprehensive regulatory information for "Philips" 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 27a37206f2c1df281a7f7e665be4bd0a and manufactured by Philips Healthcare (Suzhou) Co., Ltd. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Philips Medical Systems Nederland B.V., PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., and 5 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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