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ISO 13485 Certified  #MD 570749          

BSI, our Notified Body, was selected for the rigor they bring to the certification process and the consistency of their performance. In addition, certification by a Notified Body means that our clients can have product intended for use in the EU sterilized at BLSS knowing that their Notified Body will not require additional third party audits.

BLSS completed its first ISO 13485 certification audit in March, 2011. BSI's has found no nonconformities, verifying what our customers already know: that we provide consistent, controlled, quality EO sterilization services.

A copy of the certificate can be viewed here.

ISO 13485 Certificate MD 570794 - exp 2017
“It has been a pleasure working with you.  We hope to have product back to you as soon as we can!

Please feel free to use us as a reference - it has been a good experience.”

Rob C., Annapolis, MD

CA Device Mfr's License #53818         

The State of California inspected BLSS facilities over a period of 2 days, finding no deficiencies.
A copy of the Device Manufacturing License can be viewed here.

CA Device Manufacturer's License - 04.14 - 04.16

             “The studies are going very well! As for a good reference, I am very impressed with your services, work and knowledge.”

Alex K., Milpitas, CA


FDA Registration #3009905888