Taiwan FDA registration b165d32769cdc44291323ef14071bac1
"PROVIX" Otoscope (Non-Sterile)
TW: "波畢斯"耳鏡(未滅菌)
Taiwan·Risk Class 1·MD·PROVIX·Registered Feb 14, 2014 – Feb 14, 2019CancelledRegistration details
- Analysis ID
- b165d32769cdc44291323ef14071bac1
- License Form
- Ministry of Health Medical Device Import No. 013849
- Customs Code
- DHA09401384904
Company information
- Manufacturer
- PROVIX
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDWAY BME CORPORATION
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4770 Otoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 14, 2014
- Expiry Date
- Feb 14, 2019
- 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 "PROVIX" Otoscope (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 b165d32769cdc44291323ef14071bac1 and manufactured by PROVIX. The authorized representative in Taiwan is MEDWAY BME CORPORATION.
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