History

• 1979

  KOREA CHEMICAL EST.

• 1999

  POONGLIM PHARMATECH INCORPORATED

• 2002

  SCHOTT Schweiz AG Representative of Korea

• 2010

  KFDA'S GMP CERTIFIED MEDICAL DEVICE MANUFACTURING LICENSE

• 2014

  ISO 13485:2012 certified

• 2016

  CE certified (Sterile needle 23G*13mm & 2 others)

  Kopac launch

• 2018

  Sterile Needle FDA certified

• 2020

  CE certified(EZ-Injec 27G*13mm & 136 others)

  Saemangeum Factory 3 new construction

• 2021

  LDV Syringe, Needle FDA·CE certified

• 2022

  07COVID-19 Diagnostic Kit Launched

  07Low Dead Volume Integrated Syringe Launched in LDV

• 2023

  03KOPAC TO Syringes Launched

• 2024

  12Intravascular tube and catheter (IV) item authorization

• 2025

  12Introduction of individual representative system: Cho Mi-hee, CEO of Sales/New Product Development, Son Kwon, CEO of Manufacturing/Operation