Taiwan FDA registration a05c05ffdb608db78266b9fb7a6dd4f1
"Tin Lok" Hult analysis software
TW: “錫樂”霍特式分析軟體
Taiwan·Risk Class 2·SCHILLER AG·Registered Feb 06, 2017 – Feb 06, 2022CancelledRegistration details
- Analysis ID
- a05c05ffdb608db78266b9fb7a6dd4f1
- Customs Code
- DHA05602929809
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 Medicine Science
- Product Type (Level 2)
- E.1425 可程式設定之診斷性電腦;; E.2340 心電圖描記器
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 2017
- Expiry Date
- Feb 06, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Tin Lok" Hult analysis software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a05c05ffdb608db78266b9fb7a6dd4f1 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