Taiwan FDA registration 985350f4573b840e5195761d4b90e73f
"Cochlear" Ear manual surgical instrument (Non-Sterile)
TW: "可立耳" 耳部手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·COCHLEAR BONE ANCHORED SOLUTIONS AB·Registered Jan 03, 2014 – Jan 03, 2024ExpiredRegistration details
- Analysis ID
- 985350f4573b840e5195761d4b90e73f
- License Form
- Ministry of Health Medical Device Import No. 013744
- Customs Code
- DHA09401374403
Company information
- Manufacturer
- COCHLEAR BONE ANCHORED SOLUTIONS AB
- Manufacturer Country
- Sweden
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4420 OTOLARYNGARY Manual Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 03, 2014
- Expiry Date
- Jan 03, 2024
About this record
Access comprehensive regulatory information for "Cochlear" Ear manual surgical instrument (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 985350f4573b840e5195761d4b90e73f and manufactured by COCHLEAR BONE ANCHORED SOLUTIONS AB. The authorized representative in Taiwan is CLINICO INC..
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