Taiwan FDA registration 3b71535defd39686ae0aa5cd8d304fbd
“Bausch + Lomb”Otolaryngology Manual Surgical Instruments (Non-Sterile)
TW: “博士倫”耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·BAUSCH & LOMB INC.·Registered Sep 04, 2013 – Sep 04, 2018CancelledRegistration details
- Analysis ID
- 3b71535defd39686ae0aa5cd8d304fbd
- License Form
- Ministry of Health Medical Device Import No. 013376
- Customs Code
- DHA09401337600
Company information
- Manufacturer
- BAUSCH & LOMB INC.
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
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
- Sep 04, 2013
- Expiry Date
- Sep 04, 2018
- 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 “Bausch + Lomb”Otolaryngology Manual Surgical Instruments (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 3b71535defd39686ae0aa5cd8d304fbd and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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