Taiwan FDA registration ecc07c171ffb0a3e88ae3a1c5bac611e

"Jesset" vasodilator

TW: "杰士特"血管擴張器
Taiwan flagTaiwan·Risk Class 2·GEISTER MEDIZINTECHNIK GMBH·Registered Jan 27, 2006 – Jan 27, 2026Expired
Registration details
Analysis ID
ecc07c171ffb0a3e88ae3a1c5bac611e
Customs Code
DHA00601391504
Company information
Manufacturer Country
Germany
Authorized Representative
PLOVER MEDICAL INSTRUMENTS, INC.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Import Information
import
Dates and status
Registration Date
Jan 27, 2006
Expiry Date
Jan 27, 2026
About this record

Access comprehensive regulatory information for "Jesset" vasodilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ecc07c171ffb0a3e88ae3a1c5bac611e and manufactured by GEISTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is PLOVER 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