Taiwan FDA registration 25e0041956cd51015292759aba8beb62
"HEWEI" Manual Osteological Surgery Instrument (Unsterile)
TW: "航偉" 手動式骨科手術器械 (未滅菌)
Registration details
- Analysis ID
- 25e0041956cd51015292759aba8beb62
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hangwei Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- May 05, 2010
- Expiry Date
- May 05, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "HEWEI" Manual Osteological Surgery Instrument (Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25e0041956cd51015292759aba8beb62 and manufactured by Formosa Biomedical Technology Co., Ltd. Yilan Factory. The authorized representative in Taiwan is Hangwei Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices