Taiwan FDA registration 635f27807ed92fdf76ff8c566fd7f27d
“OLYMPUS” VISERA ELITE III VIDEO SYSTEM CENTER
TW: “奧林柏斯”影像系統主機及附件
Registration details
- Analysis ID
- 635f27807ed92fdf76ff8c566fd7f27d
- License Form
- Ministry of Health Medical Device Import No. 036803
- Customs Code
- DHA05603680300
Company information
- Manufacturer
- SHIRAKAWA OLYMPUS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 13, 2023
- Expiry Date
- Oct 13, 2028
About this record
Access comprehensive regulatory information for “OLYMPUS” VISERA ELITE III VIDEO SYSTEM CENTER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 635f27807ed92fdf76ff8c566fd7f27d and manufactured by SHIRAKAWA OLYMPUS CO., LTD.. The authorized representative in Taiwan is YUAN LI INSTRUMENT 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