Taiwan FDA registration a5acf59c5803d007070409dc322a6881
"OLYMPUS" Ear, nose, and throat examination and treatment unit (non-sterile)
TW: "奧林柏斯" 耳鼻喉檢查及治療檯 (未滅菌)
Registration details
- Analysis ID
- a5acf59c5803d007070409dc322a6881
- License Form
- Ministry of Health Medical Device Import No. 015719
- Customs Code
- DHA09401571901
Company information
- Manufacturer
- OLYMPUS WINTER & IBE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- YUAN LI INSTRUMENT 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
- Oct 05, 2015
- Expiry Date
- Oct 05, 2025
About this record
Access comprehensive regulatory information for "OLYMPUS" 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 a5acf59c5803d007070409dc322a6881 and manufactured by OLYMPUS WINTER & IBE GMBH. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices