Taiwan FDA registration 26afd88a5bdc5427d6cc838b23e2c123
"SIEMENS" DIAGNOSTIC ULTRASOUND SYSTEM
TW: "西門子" 超音波診斷系統
Registration details
- Analysis ID
- 26afd88a5bdc5427d6cc838b23e2c123
- License Form
- Department of Health Medical Device Import No. 013748
- Customs Code
- DHA00601374801
Company information
- Manufacturer
- Siemens Medical Solutions USA, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 06, 2005
- Expiry Date
- Dec 06, 2025
About this record
Access comprehensive regulatory information for "SIEMENS" DIAGNOSTIC ULTRASOUND SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26afd88a5bdc5427d6cc838b23e2c123 and manufactured by Siemens Medical Solutions USA, Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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