Taiwan FDA registration 92002cbbee69caf749f52cabd6564d8b

"Philips" patient monitor

TW: “飛利浦”病患監視器
Taiwan flagTaiwan·Risk Class 2·Philips Goldway (Shenzhen) Industrial Inc.·Registered Feb 19, 2019 – Feb 19, 2029Active
Registration details
Analysis ID
92002cbbee69caf749f52cabd6564d8b
Customs Code
DHA09200097804
Company information
Manufacturer Country
China
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Feb 19, 2019
Expiry Date
Feb 19, 2029
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About this record

Access comprehensive regulatory information for "Philips" patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92002cbbee69caf749f52cabd6564d8b and manufactured by Philips Goldway (Shenzhen) Industrial Inc.. 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 MEDIZINSYSTEME BÖBLINGEN GMBH, PHILIPS MEDICAL SYSTEMS, 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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