Taiwan FDA registration 5e68a18f38630df7625106472a853a9e
"Olympus" capsule photography system
TW: “奧林柏斯”膠囊攝影系統
Taiwan·Risk Class 2·OLYMPUS MEDICAL SYSTEMS CORPORATION HINODE PLANT·Registered Oct 01, 2009 – Oct 01, 2019CancelledRegistration details
- Analysis ID
- 5e68a18f38630df7625106472a853a9e
- Customs Code
- DHA00602021700
Company information
- Manufacturer
- OLYMPUS MEDICAL SYSTEMS CORPORATION 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 and urology
- Product Type (Level 2)
- H.1300 Swallowable Telemetry Gastrointestinal Capsule Photography System
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2009
- Expiry Date
- Oct 01, 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 "Olympus" capsule photography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e68a18f38630df7625106472a853a9e and manufactured by OLYMPUS MEDICAL SYSTEMS CORPORATION 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