Taiwan FDA registration e7f858d0c3f2dae1de83742bcf680d9c

"Philips" patient monitor

TW: “飛利浦”病患監視器
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH·Registered Sep 06, 2012 – Sep 06, 2022Cancelled
Registration details
Analysis ID
e7f858d0c3f2dae1de83742bcf680d9c
Customs Code
DHA00602394802
Company information
Manufacturer Country
Germany
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
Product Type (Level 2)
E.1025 Arrhythmia Detectors and Alerts
Import Information
import
Dates and status
Registration Date
Sep 06, 2012
Expiry Date
Sep 06, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 e7f858d0c3f2dae1de83742bcf680d9c and manufactured by PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH. 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, PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH, 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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