Taiwan FDA registration 6eb6db0ca851fe78c719b40b74354223
Megalokholt analysis software system
TW: 美地洛克霍特式分析軟體系統
Registration details
- Analysis ID
- 6eb6db0ca851fe78c719b40b74354223
- Customs Code
- DHA00602413209
Company information
- Manufacturer
- SCHILLER AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2340 Telecardiogram
- Import Information
- import
Dates and status
- Registration Date
- Oct 09, 2012
- Expiry Date
- Oct 09, 2027
About this record
Access comprehensive regulatory information for Megalokholt analysis software system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6eb6db0ca851fe78c719b40b74354223 and manufactured by SCHILLER AG. The authorized representative in Taiwan is TRUSHINE MEDICAL 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