Taiwan FDA registration 4cdda4a3b19c12c248a12d44497ec690

"Antis" injection system

TW: “安緹斯”注射系統
Taiwan flagTaiwan·Risk Class 2·ANTEIS SA·Registered Nov 14, 2012 – Nov 14, 2017Cancelled
Registration details
Analysis ID
4cdda4a3b19c12c248a12d44497ec690
Customs Code
DHA00602416501
Company information
Manufacturer
ANTEIS SA
Manufacturer Country
Switzerland
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5725 Infusion 幫浦
Import Information
import
Dates and status
Registration Date
Nov 14, 2012
Expiry Date
Nov 14, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Antis" injection system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4cdda4a3b19c12c248a12d44497ec690 and manufactured by ANTEIS SA. The authorized representative in Taiwan is MERZ ASIA PACIFIC PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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