Taiwan FDA registration 59d40b002d5afdd888743c136a31ae82
“Schiller” Easy Pulse
TW: “席樂” 宜利自動心肺復甦器
Taiwan·Risk Class 3·MD·SCHILLER AG·Registered Nov 07, 2017 – Nov 07, 2027ActiveRegistration details
- Analysis ID
- 59d40b002d5afdd888743c136a31ae82
- License Form
- Ministry of Health Medical Device Import No. 030415
- Customs Code
- DHA05603041500
Company information
- Manufacturer
- SCHILLER AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- FUTUREMED TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5200 Extracorporeal Cardiac Pressostat
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 07, 2017
- Expiry Date
- Nov 07, 2027
About this record
Access comprehensive regulatory information for “Schiller” Easy Pulse in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 59d40b002d5afdd888743c136a31ae82 and manufactured by SCHILLER AG. The authorized representative in Taiwan is FUTUREMED TECHNOLOGY CORPORATION.
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