Pure Global

JUBILANT SUNRISE SCIENTIFIC CO., LTD. - Authorized Representative in Taiwan

Explore comprehensive authorized representative profile for JUBILANT SUNRISE SCIENTIFIC CO., LTD. through Pure Global AI's free Taiwan medical device database. This authorized representative handles 20 product registrations across 14 manufacturers and 20 unique product types. Their regulatory history spans from Aug 03, 2007 to Sep 13, 2018.

This page provides detailed insights including 5 recent product registrations, 5 most popular products with “Chengdu Mechan” Plasma Surgery System having 1 registrations, and 5 represented manufacturers including SYNTHES GMBH. 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
14 Manufacturers
7 Active
13 Cancelled
JUBILANT SUNRISE SCIENTIFIC CO., LTD.
Taiwan Authorized Representative
20
Products Represented
14
Manufacturers
7
Active
Sep 2018
Latest Reg.
Pure Global
DJ Fang

DJ Fang

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Company Details

Address

臺北市內湖區洲子街79之1號4樓

Authorization Code

13092501

Recent Represented Products
Most recent products (showing top 20)

“Chengdu Mechan” Plasma Surgery System

Class 2
MD
Manufacturer: Chengdu Mechan Electronic Technology Co., Ltd.

Registered: Sep 13, 2018 • Expires: Sep 13, 2028

“SEAWON” LIBRA Inflatable Bone Expander System

Cancelled
Class 2
MD
Manufacturer: Seawon Meditech Co., Ltd.

Registered: Nov 10, 2016 • Expires: Nov 10, 2021

“SYNTHES” Prodisc-C Vivo Cervical Disc Prosthesis

Class 2
MD
Manufacturer: SYNTHES GMBH

Registered: Jul 03, 2014 • Expires: Jul 03, 2024

“SEAWON” St. Reed Steerable Neurolysis Catheter System

Class 2
MD
Manufacturer: SEAWON MEDITECH CO., LTD.

Registered: Jul 29, 2013 • Expires: Jul 29, 2023

“SEAWON” St. COX Epidural Catheter System

Class 2
MD
Manufacturer: SEAWON MEDITECH CO., LTD.

Registered: Jul 29, 2013 • Expires: Jul 29, 2023

"Weigong" rigid laryngoscope (unsterilized)

Cancelled
Class 1
Manufacturer: VYGON

Registered: Apr 11, 2012 • Expires: Apr 11, 2017

"Sindis" a new generation of artificial cervical discs

Cancelled
Class 2
Manufacturer: SYNTHES GMBH

Registered: Nov 22, 2011 • Expires: Nov 22, 2021

〝厂〞 Bone cement dispenser (sterilization)

Cancelled
Class 1
Manufacturer: WOOSUNG MEDI-FILTECH;; SEAWON MEDITECH CO., LTD.

Registered: Jul 06, 2011 • Expires: Jul 06, 2016

"Sonthek" manual instruments for general surgery (unsterilized)

Class 1
Manufacturer: SONTEC INSTRUMENTS, INC.

Registered: Jun 08, 2011 • Expires: Jun 08, 2026

"Perry Audi" Manual instruments for general surgery (unsterilized)

Cancelled
Class 1
Manufacturer: PERIOPTIX INC.

Registered: May 16, 2011 • Expires: May 16, 2016

"Hiromi" Non-powered surgical instrument (unsterilized)

Class 1
Manufacturer: PRO MED INSTRUMENTS GMBH

Registered: Mar 15, 2010 • Expires: Mar 15, 2025

"Asokol" bone vertebral body puncture needle

Cancelled
Class 2
Manufacturer: ARTHROCARE CORPORATION

Registered: Dec 10, 2009 • Expires: Dec 10, 2014

"Pushen" Paralos bone cement

Cancelled
Class 2
Manufacturer: NEUROTHERM INC.

Registered: Aug 24, 2009 • Expires: Aug 24, 2019

"Asokol" bone cement dispenser (sterilization)

Cancelled
Class 1
Manufacturer: ARTHROCARE CORPORATION

Registered: Mar 25, 2009 • Expires: Mar 25, 2014

"Asokol" manual arthroscopic equipment (unsterilized)

Cancelled
Class 1
Manufacturer: ARTHROCARE CORPORATION

Registered: Mar 25, 2009 • Expires: Mar 25, 2014

"Difu spine" Difa cervical intervertebral disc system

Cancelled
Class 3
Manufacturer: MEDOS INTERNATIONAL SARL;; Medos SARL

Registered: Feb 27, 2009 • Expires: Feb 27, 2019

"Octavia" spinal needle

Cancelled
Class 2
Manufacturer: MINRAD INC.

Registered: Feb 09, 2009 • Expires: Feb 09, 2014

"St. Francis" interspinal decompression system

Cancelled
Class 3
Manufacturer: ST. FRANCIS MEDICAL TECHNOLOGIES, INC.

Registered: Nov 25, 2008 • Expires: Nov 25, 2013

"Sindis" artificial cervical intervertebral disc

Class 2
Manufacturer: SYNTHES GMBH

Registered: Jan 08, 2008 • Expires: Jan 08, 2023

"Octavia" patient positioning beam indicator (unsterilized)

Cancelled
Class 1
Manufacturer: MINRAD INC.

Registered: Aug 03, 2007 • Expires: Aug 03, 2012