Taiwan FDA registration 644fd58d26e2907c4256cb854bd762f7

"Deutsche Boi" sphygmomanometer

TW: “德國博依”血壓計
Taiwan flagTaiwan·Risk Class 2·BEURER GMBH & CO.·Registered Apr 14, 2010 – Apr 14, 2030Active
Registration details
Analysis ID
644fd58d26e2907c4256cb854bd762f7
Customs Code
DHA00602090709
Company information
Manufacturer
BEURER GMBH & CO.
Manufacturer Country
Germany
Authorized Representative
BIOWELL HEALTH & WELL-BEING INC.
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
import
Dates and status
Registration Date
Apr 14, 2010
Expiry Date
Apr 14, 2030
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About this record

Access comprehensive regulatory information for "Deutsche Boi" sphygmomanometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 644fd58d26e2907c4256cb854bd762f7 and manufactured by BEURER GMBH & CO.. The authorized representative in Taiwan is BIOWELL HEALTH & WELL-BEING INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BEURER GMBH, 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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