Taiwan FDA registration 152482c37d53ac80ca5d14cd726f1051
Rotary peripheral angioplaster
TW: 旋轉式周邊血管成形器
Registration details
- Analysis ID
- 152482c37d53ac80ca5d14cd726f1051
- Customs Code
- DHA00600660103
Company information
- Manufacturer
- B. BRAUN MELSUNGEN AG.
- Manufacturer Country
- Germany
- Authorized Representative
- Taiwan Birlanc Co., Ltd
Product details
- Product Type (Level 1)
- 0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Mar 21, 1992
- Expiry Date
- Mar 21, 2002
- Cancellation Date
- Mar 28, 2003
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Rotary peripheral angioplaster in Taiwan's medical device market through Pure Global AI's free database. is registered under number 152482c37d53ac80ca5d14cd726f1051 and manufactured by B. BRAUN MELSUNGEN AG.. The authorized representative in Taiwan is Taiwan Birlanc Co., Ltd.
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