Taiwan FDA registration 439b69379b3a9b8f47728b2391f97579
"CHAMMED" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "查美德" 耳鼻喉光纖光源及載具(未滅菌)
Taiwan·Risk Class 1·MD·DONG-A CHAMMED CO. LTD.·Registered Dec 21, 2016 – Dec 21, 2026ActiveRegistration details
- Analysis ID
- 439b69379b3a9b8f47728b2391f97579
- License Form
- Ministry of Health Medical Device Import No. 017323
- Customs Code
- DHA09401732302
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 identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 21, 2016
- Expiry Date
- Dec 21, 2026
About this record
Access comprehensive regulatory information for "CHAMMED" Ear, nose, and throat fiberoptic light source and carrier (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 439b69379b3a9b8f47728b2391f97579 and manufactured by DONG-A CHAMMED CO. LTD.. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.
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