"Parkson" percutaneous coronary angioplasty balloon catheter
Taiwan·Risk Class 3·BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.·Registered Nov 03, 2009 – Nov 03, 2019Cancelled- Analysis ID
- 2f0cb7f5276ad731736395303c0aeafb
- Customs Code
- DHA00602029109
- Manufacturer
- BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
- 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.0005.
- Import Information
- import
- Registration Date
- Nov 03, 2009
- Expiry Date
- Nov 03, 2019
- Cancellation Date
- Jun 07, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
Access comprehensive regulatory information for "Parkson" percutaneous coronary angioplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2f0cb7f5276ad731736395303c0aeafb and manufactured by BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
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