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With the conformable design of the GORE® CARDIOFORM ASD Occluder, five catalogue numbers cover ASDs from 8 to 35 mm.*

Image
Fives sizes of GORE CARDIOFORM ASD Occluder
Catalogue numberDevice size (Disc diameter)

Treatment range measured with

stop flow balloon sizing

Sheath size
ASD27E 27 mm8-15 mm10 Fr
ASD32E32 mm13-20 mm10 Fr
ASD37E37 mm18-25 mm11 Fr
ASD44E44 mm23-30 mm12 Fr
ASD48E48 mm28-35 mm14 Fr

* Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

Recommendation for sheath size is 2 Fr larger when used with a wire.

IFU Consult instructions

Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the market where this product is available. RXOnly

INDICATIONS FOR USE IN EUROPE: The GORE® CARDIOFORM ASD Occluder is a permanently implanted device indicated for the percutaneous, transcatheter closure of ostium secundum atrial septal defects (ASDs).

CONTRAINDICATIONS: The GORE® CARDIOFORM ASD Occluder is contraindicated for use in patients:  

  • Unable to take anti-platelet or anticoagulant medications such as aspirin, heparin, or warfarin.
  • With anatomy where the GORE® CARDIOFORM ASD Occluder size or position would interfere with other intracardiac or intravascular structures, such as cardiac valves or pulmonary veins.
  • With active endocarditis, or other infections producing bacteremia, or patients with known sepsis within one month of planned implantation, or any other infection that cannot be treated successfully prior to device placement.
  • With known intracardiac thrombi. 
Product may not be available in all countries.  Please check with your Gore representative for availability.