ASTEC EN iSO 13485:2016 – IVFSynergy

ASTEC EN iSO 13485:2016

 


Newsletter


Astec acquires ISO 13485
 
We have established a quality management system for medical devices with the requirements specified in EN ISO 13485:2016
 
 
Manufacturer of high-quality laboratory instruments, designed with Japanese precision and reliability. We have dedicated ourselves to customer satisfaction throughout the years with new product engineering, customer-oriented features and an unrivaled service network of highly trained service engineers.    
 
Astec headquarters and factory in Fukuoka, Japan
 
42 years and growing
We have been in the business of incubation since 1978 and have expanded our product line to create state of the art technologies only to be admired by our competition in the market today.  







“Japanese Manufacture Astec Co ltd. has the most Stable, Spacious and Superior incubators we have seen in the market so far!”     
             
I.R.I Science Report Magazine Feb, 2019







A Special Announcement
 
EC6S-MD
FDA Class II device listing
We are proud to announce that ASTEC has been listed with the FDA as a medical device manufacturer in the United States of America!
 


Introducing the EC6S-MD now with a Medical Device License
Class IIa
93/42/EEC Annex V
Designed and Made in Japan








THE 35TH ANNUAL MEETING ESHRE
 
VIENNA- AUSTRIA 23 – 26 JUNE
Booth# E77
 
Dear Sir/Madam,
It is our distinct pleasure to invite you and your colleagues to attend the 35th Annual Meeting of European Society of Human Reproduction and Embryology which will be held in Vienna, Austria, from 23 to 26 June 2019, where we will display our latest technology and breakthrough products throughout the event.
On behalf of the entire ASTEC Bio team we wish you and your family a safe journey to Vienna and sincerely look forward to meeting you soon.
Best Regards,
 
Takeo Cho  / General Manager of Global Division  




 
Astec Global Presence

Share this post



← Older Post Newer Post →


Leave a comment

Please note, comments must be approved before they are published.