On Feb. 26th, 2013, the HeartR ASD/PDA Occluder and SteerEase Introducer manufactured by Lifetech got approval in Uzbekistan on Aug. 16th and Aug. 30th respectively, which means these products can be advanced into Uzbekistan.
On June 24th, 2013, the product of LawMax Dilator manufactured by Lifetech received 510k submission from FDA, which means the product has been permitted to market into the American.
On June 21st, 2013, the Ankura Stent Graft System manufactured by Lifetech got approval by MOH in Hong Kong, which means this product can be advanced into Hong Kong market.
On April 11th, 2013, the AegeisyTM Vena Cava Filter manufactured by Lifetech got approval by MOH in Australia, which means this product can be advanced into Australia market.
On Apr. 09th, 2013, the Cera VSD Occluder manufactured by Lifetech got approval in Thailand, which means this product can be advanced into Thailand market.
On March 28th, 2013, the LungPoint Software manufactured by Broncus got approval by MOH in Hong Kong, which means this product can be advanced into Hong Kong market
On Feb. 26th, 2013, the Cera ASD Occluder and CeraTM PDA Occluder manufactured by Lifetech got approval in Thailand, which means this product can be advanced into Thailand market.
On Dec. 24, 2012, Lifetech Cera ASD Occluder and CeraTM PDA Occluder have got SFDA Registration Certificate, it means these products of Lifetech have been approved to market into China.
On Dec. 24, 2012, Lifetech Cera?ASD Occluder and CeraTM PDA Occluder have got SFDA Registration Certificate, it means these products of Lifetech have been approved to market into China.
On October 29th 2012, SpiderTM PFO Closure System and LawMaxTM Dilator got European CE Mark approval, which marks the success for advancing into European market.