Taiwan FDA registration bebe5275d7da31db6f12167e74e6429f
"HK" Ear, nose, and throat manual surgical instrument (Non-Sterile)
TW: "弘光" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·HK SURGICAL INC.·Registered Oct 16, 2015 – Oct 16, 2020CancelledRegistration details
- Analysis ID
- bebe5275d7da31db6f12167e74e6429f
- License Form
- Ministry of Health Medical Device Import No. 015746
- Customs Code
- DHA09401574604
Company information
- Manufacturer
- HK SURGICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- Youjian Mengwei Biomedical Co., Ltd
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4420 OTOLARYNGARY Manual Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 16, 2015
- Expiry Date
- Oct 16, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for "HK" Ear, nose, and throat manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bebe5275d7da31db6f12167e74e6429f and manufactured by HK SURGICAL INC.. The authorized representative in Taiwan is Youjian Mengwei Biomedical Co., Ltd.
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