Taiwan FDA registration 7727c9dacb469f3f4b564422270f03ea
"Belsen" Kema coronary stent system
TW: “百爾森”克瑪冠狀動脈支架系統
Taiwan·Risk Class 3·BIOSENSORS EUROPE SA;; BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.·Registered Nov 26, 2019 – Nov 26, 2029ActiveRegistration details
- Analysis ID
- 7727c9dacb469f3f4b564422270f03ea
- Customs Code
- DHA05603304508
Company information
- Manufacturer Country
- Switzerland;;Singapore
- Authorized Representative
- K&C MEDICAL CO., LTD.
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.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Nov 26, 2019
- Expiry Date
- Nov 26, 2029
About this record
Access comprehensive regulatory information for "Belsen" Kema coronary stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7727c9dacb469f3f4b564422270f03ea and manufactured by BIOSENSORS EUROPE SA;; BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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