Taiwan FDA registration a4048e5eed26309ec973b835cf5d0857
"Schiller" Depeck defluttered the monitor
TW: “席勒”德培克去顫監視器
Registration details
- Analysis ID
- a4048e5eed26309ec973b835cf5d0857
- Customs Code
- DHA00602448503
Company information
- Manufacturer
- SCHILLER MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- HI-CLEARANCE INC.
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.5310 自動體外去顫器系統
- Import Information
- import
Dates and status
- Registration Date
- Feb 27, 2013
- Expiry Date
- Feb 27, 2023
About this record
Access comprehensive regulatory information for "Schiller" Depeck defluttered the monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a4048e5eed26309ec973b835cf5d0857 and manufactured by SCHILLER MEDICAL. The authorized representative in Taiwan is HI-CLEARANCE 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