Taiwan FDA registration c015b7397236db381cd51037b1dd36f0

“CHAMMED” Ear, nose and throat examination and treatment unit (Non-Sterile)

TW: “查美德” 耳鼻喉檢查及治療檯 (未滅菌)

Taiwan·Risk Class 1·MD·DONG-A CHAMMED CO. LTD.·Registered Nov 28, 2016 – Nov 28, 2026Active

Registration details

Analysis ID: c015b7397236db381cd51037b1dd36f0
License Form: Ministry of Health Medical Device Import No. 017221
Customs Code: DHA09401722104

Company information

Manufacturer: DONG-A CHAMMED CO. LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: BOYANG MEDICAL TECHNOLOGY CO., LTD

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: Nov 28, 2016
Expiry Date: Nov 28, 2026

About this record

Access comprehensive regulatory information for “CHAMMED” 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 c015b7397236db381cd51037b1dd36f0 and manufactured by DONG-A CHAMMED CO. LTD.. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

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