Taiwan FDA registration 61ccfaf84351c870f5c5e44ba20088f6
PACH Anterior Lumbar Plate System
TW: 倍脊腰椎前路骨板系統
Taiwan·Risk Class 2·MD·Guanya Biotechnology Co., Ltd. new store factory·Registered Aug 01, 2016 – Aug 01, 2021CancelledRegistration details
- Analysis ID
- 61ccfaf84351c870f5c5e44ba20088f6
- License Form
- Ministry of Health Medical Device Manufacturing No. 005386
Company information
- Manufacturer
- Guanya Biotechnology Co., Ltd. new store factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A-SPINE Asia Co., Ltd.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 01, 2016
- Expiry Date
- Aug 01, 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 PACH Anterior Lumbar Plate System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61ccfaf84351c870f5c5e44ba20088f6 and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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