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“OLYMPUS” Evis Lucera Elite Bronchofibervideoscope - Taiwan Registration 233573d8a2c0b7f18eb78857dd9a2505

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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233573d8a2c0b7f18eb78857dd9a2505
Registration Details
Taiwan FDA Registration: 233573d8a2c0b7f18eb78857dd9a2505
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Device Details

“OLYMPUS” Evis Lucera Elite Bronchofibervideoscope
TW: “奧林柏斯”電子式細鏡支氣管鏡
Risk Class 2
MD

Registration Details

233573d8a2c0b7f18eb78857dd9a2505

Ministry of Health Medical Device Import No. 031391

DHA05603139104

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT device

G4680 Bronchoscope (soft or rigid) and accessories

Imported from abroad

Dates and Status

Aug 08, 2018

Aug 08, 2028