Taiwan FDA registration 36948eb1ec57ea795e2d80a23066232a
"Berty" Central Venous Catheter Group
TW: “柏蒂” 中央靜脈導管組
Taiwan·Risk Class 2·Bioptimal International Pte. Ltd.·Registered Oct 24, 2011 – Oct 24, 2021CancelledRegistration details
- Analysis ID
- 36948eb1ec57ea795e2d80a23066232a
- Customs Code
- DHA00602290301
Company information
- Manufacturer
- Bioptimal International Pte. Ltd.
- Manufacturer Country
- Singapore
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- import
Dates and status
- Registration Date
- Oct 24, 2011
- Expiry Date
- Oct 24, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Berty" Central Venous Catheter Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36948eb1ec57ea795e2d80a23066232a and manufactured by Bioptimal International Pte. Ltd.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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