Taiwan FDA registration 12c0164b6394f5c67af6d587b6663034
"Jesset" cardiovascular surgery instrument (unsterilized)
TW: “傑士特”心臟血管外科器械 (未滅菌)
Registration details
- Analysis ID
- 12c0164b6394f5c67af6d587b6663034
- Customs Code
- DHA04400660202
Company information
- Manufacturer
- GEISTER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- VIATRON MEDICAL INSTRUMENTS INC.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- import
Dates and status
- Registration Date
- Mar 25, 2008
- Expiry Date
- Mar 25, 2013
- Cancellation Date
- Jun 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jesset" cardiovascular surgery instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 12c0164b6394f5c67af6d587b6663034 and manufactured by GEISTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is VIATRON MEDICAL INSTRUMENTS 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