Taiwan FDA registration 86426f365b5b8bf1c821c3456e559bd6
“Technolas Perfect Vision” Zyoptix Diagnostic Workstation 3
TW: “得克樂視” 佳威安保視眼球診斷系統儀3
Taiwan·Risk Class 2·MD·TECHNOLAS PERFECT VISION GMBH·Registered Aug 04, 2015 – Aug 04, 2020CancelledRegistration details
- Analysis ID
- 86426f365b5b8bf1c821c3456e559bd6
- License Form
- Ministry of Health Medical Device Import No. 027579
- Customs Code
- DHA05602757907
Company information
- Manufacturer
- TECHNOLAS PERFECT VISION GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- CHIU HO SCIENTIFIC CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1850 AC power type fine gap lamp
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 04, 2015
- Expiry Date
- Aug 04, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Technolas Perfect Vision” Zyoptix Diagnostic Workstation 3 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 86426f365b5b8bf1c821c3456e559bd6 and manufactured by TECHNOLAS PERFECT VISION GMBH. The authorized representative in Taiwan is CHIU HO SCIENTIFIC 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