Taiwan FDA registration a131b7c27378bf972837028b0c549938
"Dibo" casing
TW: “帝寶”套管
Taiwan·Risk Class 2·THIEBAUD S.A.S·Registered Sep 19, 2011 – Sep 19, 2021CancelledRegistration details
- Analysis ID
- a131b7c27378bf972837028b0c549938
- Customs Code
- DHA00602281501
Company information
- Manufacturer
- THIEBAUD S.A.S
- Manufacturer Country
- France
- Authorized Representative
- GALDERMA HONG KONG LIMITED, TAIWAN BRANCH
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.5570 Subcutaneous single-chamber needle
- Import Information
- import
Dates and status
- Registration Date
- Sep 19, 2011
- Expiry Date
- Sep 19, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Dibo" casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a131b7c27378bf972837028b0c549938 and manufactured by THIEBAUD S.A.S. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.
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