Taiwan FDA registration 561a82c8289886bcf9b12886e365ddc6
"Shengmai" funnel chest correction plate device
TW: "生邁"漏斗胸矯正板器械
Taiwan·Risk Class 2·BIOMET ORTHOPEDICS, INC.;; BIOMET MICROFIXATION·Registered Jul 21, 2006 – Jul 21, 2021CancelledRegistration details
- Analysis ID
- 561a82c8289886bcf9b12886e365ddc6
- Customs Code
- DHA00601690401
Company information
- Manufacturer
- BIOMET ORTHOPEDICS, INC.;; BIOMET MICROFIXATION
- Manufacturer Country
- United States
- Authorized Representative
- Yangzhi Biotechnology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- import
Dates and status
- Registration Date
- Jul 21, 2006
- Expiry Date
- Jul 21, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Shengmai" funnel chest correction plate device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 561a82c8289886bcf9b12886e365ddc6 and manufactured by BIOMET ORTHOPEDICS, INC.;; BIOMET MICROFIXATION. The authorized representative in Taiwan is Yangzhi Biotechnology Co., Ltd.
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