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“Takara Belmont” Ear, nose and throat examination and treatment unit (Non-Sterile) - Taiwan Registration 5e270464e955d9e765c6725e103f79cb

Access comprehensive regulatory information for “Takara Belmont” Ear, nose and throat examination and treatment unit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e270464e955d9e765c6725e103f79cb and manufactured by TAKARA BELMONT CORPORATION – OSAKA FACTORY. The authorized representative in Taiwan is TAKARA BELMONT (TAIWAN) CORPORATION.

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5e270464e955d9e765c6725e103f79cb
Registration Details
Taiwan FDA Registration: 5e270464e955d9e765c6725e103f79cb
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Device Details

“Takara Belmont” Ear, nose and throat examination and treatment unit (Non-Sterile)
TW: "寶貝蒙” 耳鼻喉檢查及治療檯 (未滅菌)
Risk Class 1
MD

Registration Details

5e270464e955d9e765c6725e103f79cb

Ministry of Health Medical Device Import No. 018413

DHA09401841305

Company Information

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".

G ENT device

G5300 ENT Examination and Treatment Unit

Imported from abroad

Dates and Status

Oct 17, 2017

Oct 17, 2027