Taiwan FDA registration 5e270464e955d9e765c6725e103f79cb
“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)
Taiwan·Risk Class 1·MD·TAKARA BELMONT CORPORATION – OSAKA FACTORY·Registered Oct 17, 2017 – Oct 17, 2027ActiveRegistration details
- Analysis ID
- 5e270464e955d9e765c6725e103f79cb
- License Form
- Ministry of Health Medical Device Import No. 018413
- Customs Code
- DHA09401841305
Company information
- Manufacturer
- TAKARA BELMONT CORPORATION – OSAKA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TAKARA BELMONT (TAIWAN) CORPORATION
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G5300 ENT Examination and Treatment Unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 17, 2017
- Expiry Date
- Oct 17, 2027
About this record
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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