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FDA Indication for MyoSure
 
 
FDA clears the Myosure® system for a new indication - the removal of retained products of conception.

   
Retained products of conception (RPOC) is non-viable pregnancy tissue that has not passed due to:
- Failed expectant management.
- Post treatment of miscarriage.
- Term delivery.
   
Traditional D&C is the most common treatment for RPOC,
but the data shows:
- Increased risk of perforation, infection and bleeding.1
- 19% incidence of adhesion formation after D&C.2
- Up to 32% incidence of adhesion formation after multiple D&C procedures.2
   

   
The MyoSure system is a solution for the removal of RPOC:
- Remove only the targeted tissue.
- Reduced risk of damage to healthy tissue.
- Direct visualization for confirmation of removal.
   

 

 

  RESOURCES  
 

Offer your patients the best treatment option, while preserving their future fertility.  

 
     
 

Watch a video
http://youtu.be/tah9FYGwhsc

 
     
 

Case study of the MyoSure system use for removal of retained products of conception
http://hologiced.com/clinical-category/hts/

 
     
 

Learn more about the MyoSure system MyoSure.com

 
     

   
 

1. Sadan O, et al. Role of sonography in the diagnosis of retained products of conception. J Ultrasound Med 2004; 23:371-74. 2. Friedler S, Margaloioth EJ, Kafka I, Yaffe H. Incidence of post-abortion intra-uterine adhesions evaluated by hysteroscopy-a-prospective study. Hum Reprod. 1993;8:442-444

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