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"Deutsche Boi" sphygmomanometer - Taiwan Registration 11fc8aee1f9d277af2988dfed1e344a6

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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11fc8aee1f9d277af2988dfed1e344a6
Registration Details
Taiwan FDA Registration: 11fc8aee1f9d277af2988dfed1e344a6
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Device Details

"Deutsche Boi" sphygmomanometer
TW: โ€œๅพทๅœ‹ๅšไพโ€่ก€ๅฃ“่จˆ
Risk Class 2
Cancelled

Registration Details

11fc8aee1f9d277af2988dfed1e344a6

DHA00602091600

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1130.

import

Dates and Status

Apr 20, 2010

Apr 20, 2020

Jul 15, 2022

Cancellation Information

Logged out

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