Taiwan FDA registration 11fc8aee1f9d277af2988dfed1e344a6

"Deutsche Boi" sphygmomanometer

TW: “德國博依”血壓計
Taiwan flagTaiwan·Risk Class 2·BEURER GMBH·Registered Apr 20, 2010 – Apr 20, 2020Cancelled
Registration details
Analysis ID
11fc8aee1f9d277af2988dfed1e344a6
Customs Code
DHA00602091600
Company information
Manufacturer
BEURER GMBH
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 20, 2010
Expiry Date
Apr 20, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 11fc8aee1f9d277af2988dfed1e344a6 and manufactured by BEURER GMBH. The authorized representative in Taiwan is BIOWELL HEALTH & WELL-BEING INC..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BEURER GMBH, BEURER GMBH & CO., 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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