Taiwan FDA registration cd085b92bc164055ab3dda7ce1303442
“OLYMPUS” VISERA TRANSNASAL ESOPHAGOVIDEOSCOPE AND ACCESSORIES
TW: “奧林柏斯”食道電子內視鏡及附件
Taiwan·Risk Class 2·MD·AIZU OLYMPUS CO., LTD·Registered Jan 04, 2022 – Jan 04, 2027ActiveRegistration details
- Analysis ID
- cd085b92bc164055ab3dda7ce1303442
- License Form
- Ministry of Health Medical Device Import No. 035173
- Customs Code
- DHA05603517301
Company information
- Manufacturer
- AIZU 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
- Jan 04, 2022
- Expiry Date
- Jan 04, 2027
About this record
Access comprehensive regulatory information for “OLYMPUS” VISERA TRANSNASAL ESOPHAGOVIDEOSCOPE AND ACCESSORIES in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cd085b92bc164055ab3dda7ce1303442 and manufactured by AIZU 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