Taiwan FDA registration 02f2426ccf857d226fb7541fc7d0fd24

Dr. Pulse electronic blood pressure monitor

TW: 脈博士電子血壓計
Taiwan flagTaiwan·Risk Class 2·GMC Inc.·Registered Jul 25, 2019 – Jul 25, 2029Active
Registration details
Analysis ID
02f2426ccf857d226fb7541fc7d0fd24
Customs Code
DHA09200105309
Company information
Manufacturer
GMC Inc.
Manufacturer Country
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
Input;; Chinese goods
Dates and status
Registration Date
Jul 25, 2019
Expiry Date
Jul 25, 2029
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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 02f2426ccf857d226fb7541fc7d0fd24 and manufactured by GMC Inc.. 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, Yousheng Medical Technology Co., Ltd. Neihu No. 2 Factory, 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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