Taiwan FDA registration f5638bf64324f4c3684c01243138dbf9
"Byrean" extrafixation system
TW: "拜雷安" 腦神外固定系統
Taiwan·Risk Class 2·BIOPLATE, INC.·Registered May 30, 2001 – May 30, 2021CancelledRegistration details
- Analysis ID
- f5638bf64324f4c3684c01243138dbf9
- Customs Code
- DHA00600967202
Company information
- Manufacturer
- BIOPLATE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ASIAMED INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5330 Preformed non-changeable head skullforming plate
- Import Information
- import
Dates and status
- Registration Date
- May 30, 2001
- Expiry Date
- May 30, 2021
- Cancellation Date
- Sep 11, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Byrean" extrafixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5638bf64324f4c3684c01243138dbf9 and manufactured by BIOPLATE, INC.. The authorized representative in Taiwan is ASIAMED INSTRUMENTS CO., LTD..
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