Taiwan FDA registration 233573d8a2c0b7f18eb78857dd9a2505
“OLYMPUS” Evis Lucera Elite Bronchofibervideoscope
TW: “奧林柏斯”電子式細鏡支氣管鏡
Taiwan·Risk Class 2·MD·AIZU OLYMPUS CO., LTD·Registered Aug 08, 2018 – Aug 08, 2028ActiveRegistration details
- Analysis ID
- 233573d8a2c0b7f18eb78857dd9a2505
- License Form
- Ministry of Health Medical Device Import No. 031391
- Customs Code
- DHA05603139104
Company information
- Manufacturer
- AIZU OLYMPUS CO., LTD
- 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)
- G ENT device
- Product Type (Level 2)
- G4680 Bronchoscope (soft or rigid) and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 08, 2018
- Expiry Date
- Aug 08, 2028
About this record
Access comprehensive regulatory information for “OLYMPUS” Evis Lucera Elite Bronchofibervideoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 233573d8a2c0b7f18eb78857dd9a2505 and manufactured by AIZU OLYMPUS CO., LTD. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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