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"Pentax" ultrasound electronic bronchoscope - Taiwan Registration cb75835b448863fc9eabf9f9172c4d19

Access comprehensive regulatory information for "Pentax" ultrasound electronic bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb75835b448863fc9eabf9f9172c4d19 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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cb75835b448863fc9eabf9f9172c4d19
Registration Details
Taiwan FDA Registration: cb75835b448863fc9eabf9f9172c4d19
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Device Details

"Pentax" ultrasound electronic bronchoscope
TW: โ€œ่ณ“ๅพ—ๅฃซโ€่ถ…้Ÿณๆณข้›ปๅญๅผๆ”ฏๆฐฃ็ฎก้ก
Risk Class 2

Registration Details

cb75835b448863fc9eabf9f9172c4d19

DHA00602060009

Product Details

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

G ENT Science

G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof

import

Dates and Status

Feb 25, 2010

Feb 25, 2025