Taiwan FDA registration 67a127be98e9bb064a2282c71f472daf
"OLYMPUS" ENDOCAPSULE 10 System-Software
TW: "奧林柏斯"膠囊內視鏡系統-軟體
Taiwan·Risk Class 2·MD·Olympus Medical Systems Corp. Hinode Plant·Registered May 28, 2015 – May 28, 2025ExpiredRegistration details
- Analysis ID
- 67a127be98e9bb064a2282c71f472daf
- License Form
- Ministry of Health Medical Device Import No. 027403
- Customs Code
- DHA05602740309
Company information
- Manufacturer
- Olympus Medical Systems Corp. Hinode Plant
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1300 Swallowable Telemetry Gastrointestinal Capsule Photography System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2015
- Expiry Date
- May 28, 2025
About this record
Access comprehensive regulatory information for "OLYMPUS" ENDOCAPSULE 10 System-Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67a127be98e9bb064a2282c71f472daf and manufactured by Olympus Medical Systems Corp. Hinode Plant. 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