Taiwan FDA registration 7969e204bed1ca6b322ae257c13a2694
“Bausch + Lomb”Manual Ophthalmic Surgical Instruments(Non-Sterile)
TW: “博士倫”手動式眼科手術器械(未滅菌)
Taiwan·Risk Class 1·MD·BAUSCH & LOMB INC.·Registered Sep 04, 2013 – Sep 04, 2018CancelledRegistration details
- Analysis ID
- 7969e204bed1ca6b322ae257c13a2694
- License Form
- Ministry of Health Medical Device Import No. 013377
- Customs Code
- DHA09401337702
Company information
- Manufacturer
- BAUSCH & LOMB INC.
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4350 Manual Ophthalmic Surgery 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”Manual Ophthalmic 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 7969e204bed1ca6b322ae257c13a2694 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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