Pure Global

"Deutsche Boi" sphygmomanometer - Taiwan Registration 7db38722692eb07690294eba276e7661

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 7db38722692eb07690294eba276e7661 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
2 Competitors
3 Recent Registrations
7db38722692eb07690294eba276e7661
Registration Details
Taiwan FDA Registration: 7db38722692eb07690294eba276e7661
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

7db38722692eb07690294eba276e7661

DHA00602391905

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

Aug 10, 2012

Aug 10, 2017

Nov 28, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ

Companies Making Similar Products
Top companies providing products similar to ""Deutsche Boi" sphygmomanometer"