"Deutsche Boi" sphygmomanometer
Taiwan·Risk Class 2·BEURER GMBH·Registered Aug 10, 2012 – Aug 10, 2017Cancelled- Analysis ID
- 7db38722692eb07690294eba276e7661
- Customs Code
- DHA00602391905
- Manufacturer
- BEURER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOWELL HEALTH & WELL-BEING INC.
- 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
- Registration Date
- Aug 10, 2012
- Expiry Date
- Aug 10, 2017
- Cancellation Date
- Nov 28, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.