Taiwan FDA registration 0c5390247edc9c71301934c2ac56dfce
"KENZ" Manual Stethoscope (Non-sterile)
TW: "肯士" 手動聽診器 (未滅菌)
Taiwan·Risk Class 1·MD·KENZMEDICAL CO., LTD.·Registered Feb 07, 2014 – Feb 07, 2024ExpiredRegistration details
- Analysis ID
- 0c5390247edc9c71301934c2ac56dfce
- License Form
- Ministry of Health Medical Device Import No. 013837
- Customs Code
- DHA09401383700
Company information
- Manufacturer
- KENZMEDICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDWAY BME CORPORATION
Product details
- Intended Use
- Limited to the first-level identification range of the "stethoscope (E.1875)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1875 stethoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 07, 2014
- Expiry Date
- Feb 07, 2024
About this record
Access comprehensive regulatory information for "KENZ" Manual Stethoscope (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c5390247edc9c71301934c2ac56dfce and manufactured by KENZMEDICAL CO., LTD.. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
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