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"Pentax" electronic esophageal endoscope - Taiwan Registration 46c3a122c54f3118be0778ba719f5d9f

Access comprehensive regulatory information for "Pentax" electronic esophageal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46c3a122c54f3118be0778ba719f5d9f 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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46c3a122c54f3118be0778ba719f5d9f
Registration Details
Taiwan FDA Registration: 46c3a122c54f3118be0778ba719f5d9f
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Device Details

"Pentax" electronic esophageal endoscope
TW: โ€œ่ณ“ๅพ—ๅฃซโ€้›ปๅญๅผ้ฃŸ้“ๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

46c3a122c54f3118be0778ba719f5d9f

DHA00601877602

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Apr 03, 2008

Apr 03, 2028