Taiwan FDA registration 7184318c15102a39820e3d5e9eb2e462
"Pusen" blood pressure monitoring kit
TW: "普生" 血壓監視套組
Registration details
- Analysis ID
- 7184318c15102a39820e3d5e9eb2e462
- Customs Code
- DHA00601015903
Company information
- Manufacturer
- PULSION MEDICAL SYSTEMS SE
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Dec 18, 2002
- Expiry Date
- Dec 18, 2027
- Cancellation Date
- Nov 22, 2012
About this record
Access comprehensive regulatory information for "Pusen" blood pressure monitoring kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7184318c15102a39820e3d5e9eb2e462 and manufactured by PULSION MEDICAL SYSTEMS SE. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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