Taiwan FDA registration 7d1e9610880e002ec3c5d34e48f1722d

Dr. Pulse electronic blood pressure monitor

TW: 脈博士電子血壓計
Taiwan flagTaiwan·Risk Class 2·Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory·Registered Aug 16, 2010 – Aug 16, 2025Cancelled
Registration details
Analysis ID
7d1e9610880e002ec3c5d34e48f1722d
Customs Code
DHY00500307706
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
ROSSMAX INTERNATIONAL LTD.
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.1130.
Import Information
Domestic
Dates and status
Registration Date
Aug 16, 2010
Expiry Date
Aug 16, 2025
Cancellation Date
Jul 10, 2020
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for Dr. Pulse electronic blood pressure monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d1e9610880e002ec3c5d34e48f1722d and manufactured by Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory. The authorized representative in Taiwan is ROSSMAX INTERNATIONAL LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including ROSSMAX (SHANGHAI) INCORPORATION LTD, GMC Inc., and 3 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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