Taiwan FDA registration f934cd5c235c3debeef82e1918579926
"Medikro" Breathing Mouthpiece (Non-Sterile)
TW: "美迪克" 呼吸咬嘴 (未滅菌)
Taiwan·Risk Class 1·MD·MEDIKRO OY·Registered Dec 01, 2016 – Dec 01, 2021ExpiredRegistration details
- Analysis ID
- f934cd5c235c3debeef82e1918579926
- License Form
- Ministry of Health Medical Device Import No. 017238
- Customs Code
- DHA09401723808
Company information
- Manufacturer
- MEDIKRO OY
- Manufacturer Country
- Finland
- Authorized Representative
- SHIN CHEN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Bites (D.5620)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5620 Breathing bite
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 01, 2016
- Expiry Date
- Dec 01, 2021
About this record
Access comprehensive regulatory information for "Medikro" Breathing Mouthpiece (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 f934cd5c235c3debeef82e1918579926 and manufactured by MEDIKRO OY. The authorized representative in Taiwan is SHIN CHEN 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