Taiwan FDA registration 0950ce9c1b486c11ccd5095a82636e5c
“Medikro” Spirometer
TW: “美迪克”肺量計
Taiwan·Risk Class 2·MD·MEDIKRO OY·Registered Nov 06, 2017 – Nov 06, 2022ExpiredRegistration details
- Analysis ID
- 0950ce9c1b486c11ccd5095a82636e5c
- License Form
- Ministry of Health Medical Device Import No. 030411
- Customs Code
- DHA05603041105
Company information
- Manufacturer
- MEDIKRO OY
- Manufacturer Country
- Finland
- Authorized Representative
- SHIN CHEN INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D1840 Spirometer for diagnosis
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 06, 2017
- Expiry Date
- Nov 06, 2022
About this record
Access comprehensive regulatory information for “Medikro” Spirometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0950ce9c1b486c11ccd5095a82636e5c 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