Taiwan FDA registration 493a0b65c2feacb861aadc176e2f0d73
"Medicon" Prosthesis modification instrument for ossicular replacement surgery (Non-sterile)
TW: "美笛康" 聽小骨置換物修正用器械 (未滅菌)
Taiwan·Risk Class 1·MD·MEDICON EG·Registered Feb 14, 2023 – Feb 14, 2028ActiveRegistration details
- Analysis ID
- 493a0b65c2feacb861aadc176e2f0d73
- License Form
- Ministry of Health Medical Device Import No. 023042
- Customs Code
- DHA09402304203
Company information
- Manufacturer
- MEDICON EG
- Manufacturer Country
- Germany
- Authorized Representative
- GOLDENSPRING MEDI-TECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Classification and Grading Management Measures for Medical Devices "Devices for Correction of Small Bone Replacement (G.3540)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G3540 Instrument for Hearing Bone Replacement Correction
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 14, 2023
- Expiry Date
- Feb 14, 2028
About this record
Access comprehensive regulatory information for "Medicon" Prosthesis modification instrument for ossicular replacement surgery (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 493a0b65c2feacb861aadc176e2f0d73 and manufactured by MEDICON EG. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..
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