Pure Global

Xiongqun Enterprise Limited - Authorized Representative in Taiwan

Explore comprehensive authorized representative profile for Xiongqun Enterprise Limited through Pure Global AI's free Taiwan medical device database. This authorized representative handles 20 product registrations across 6 manufacturers and 19 unique product types. Their regulatory history spans from Jun 14, 1996 to Jun 30, 2005.

This page provides detailed insights including 5 recent product registrations, 5 most popular products with "Keithley" implanted cardiac remediator having 2 registrations, and 5 represented manufacturers including GUIDANT IRELAND. Pure Global AI offers free access to Taiwan's medical device database, enabling global MedTech companies to analyze market dynamics and identify opportunities.

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20 Products
6 Manufacturers
20 Cancelled
Xiongqun Enterprise Limited
Taiwan Authorized Representative
20
Products Represented
6
Manufacturers
0
Active
Jun 2005
Latest Reg.
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Company Details

Address

台北市中山區松江路131號5樓

Authorization Code

04549450

Recent Represented Products
Most recent products (showing top 20)

"Kaiden" Flygt steroid-eluting stretchable/retractable spiral coil rhythm/induction wires

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Jun 30, 2005 • Expires: Apr 21, 2010

"Keithley" Kant dual-chamber synchronous rectifier/defibrillator

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Mar 23, 2005 • Expires: Apr 21, 2010

"Kaiden" Hiloh geoatrial bipolar lead

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Dec 20, 2004 • Expires: Apr 21, 2010

"Keithley" Kant's Rectifier

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Nov 03, 2004 • Expires: Apr 21, 2010

"Keithley" Silo Pi can get the catheter

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Jul 15, 2004 • Expires: Apr 21, 2010

"Keithley" Vigorous implantable heart rhythm rectifier defibrillator

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Apr 05, 2004 • Expires: Apr 21, 2010

"Keithley" implanted cardiac remediator

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Sep 18, 2003 • Expires: Apr 21, 2010

"Kaidiland" Finnish wire

Cancelled
Manufacturer: GUIDANT CORPORATION

Registered: Feb 12, 2003 • Expires: Apr 21, 2010

"Keithley" Ender Lilly implanted with fibrillation wires

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Sep 12, 2002 • Expires: Apr 21, 2010

"Keithley" Billy implantable heart rhythm rectifier defibrillator

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Aug 07, 2002 • Expires: Apr 21, 2010

"Kaiden" Hiloh Atrial J-lead

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Jul 04, 2002 • Expires: Apr 21, 2010

"Keithley" implanted cardiac remediator

Cancelled
Manufacturer: GUIDANT IRELAND

Registered: Mar 26, 2002 • Expires: Apr 21, 2010

Program adjustment record monitor for artificial heart rhythm

Cancelled
Manufacturer: GUIDANT CORPORATION

Registered: Aug 30, 2001 • Expires: Apr 21, 2010

Punk implantable heart rhythm rectifier defibrillator

Cancelled
Manufacturer: GUIDANT-CARDIAC PACEMAKERS

Registered: May 31, 1999 • Expires: Apr 21, 2010

conducting wire

Cancelled
Manufacturer: GUIDANT-CARDIAC PACEMAKERS

Registered: May 17, 1999 • Expires: Apr 21, 2010

Implanted cardiac rectifier

Cancelled
Manufacturer: GUIDANT-CARDIAC PACEMAKERS

Registered: Dec 09, 1998 • Expires: Apr 21, 2010

Blood dehydrator

Cancelled
Manufacturer: MINNTECH CORPORATION

Registered: Oct 01, 1998 • Expires: Apr 21, 2010

Implantable rhythm rectifier defibrillator

Cancelled
Manufacturer: GUIDANT-CARDIAC PACEMKERS.

Registered: Apr 08, 1997 • Expires: Apr 21, 2010

Artificial heart-lung

Cancelled
Manufacturer: MINNTECH CORPORATION

Registered: Dec 11, 1996 • Expires: Apr 21, 2010

Membrane artificial heart-lung

Cancelled
Manufacturer: BARD VASCULAR SYSTEMS DIVISION C.R. BARD INC.

Registered: Jun 14, 1996 • Expires: Apr 21, 2010