Cocoon PFO Occluder

Cocoon PFO Occluder

Extensive size matrix so that there is no compromise

6 SKUs
(vs 4 SKUs of the competitor)

5 out of 6 occluders are 8F sheath compatible

Softness to protect

2+ times softer at the rims

Designed to minimize nickel leaching

Platinum nanocoating

Extensive size matrix so that there is no compromise 6 SKUs (vs 4 SKUs of competitor)

Softness to Protect 2+ times softer at the rims

Displacement at 1.0 mm

Displacement at 1.5 mm

5 out of 6 occluders are 8F sheath compatible

5 out of 6 occluders are 8F sheath compatible

Designed to minimize nickel leaching
Platinum nanocoating

  • Ultrathin layer of Platinum atoms using nanofusion technology is coated on the Nitinol wire by a process called plasma deposition
  • Platinum nanocoating makes the Cocoon Occluders inert, biocompatible, non-corrosive and non-allergic and also enhances radiopacity

Raw nitinol

Electropolished

Platinum nanocoating

Platinum nanocoating makes the Cocoon PFO Occluder:

Device Description

Design

  • Right atrial disc diameter (Ø1)
  • Left atrial disc diameter (Ø2)
  • Waist length (L1)
  • Total length (L2)

Technical Specifications

Catalog number Right atrial disc diameter (Ø1)
(mm)
Left atrial disc diameter (Ø2)
(mm)
Waist length (L1)
(mm)
Total length (L2)
(mm)
Sheath Size (F) Cable Code
CPF1818183586
CPF2525183586
CPF252525253586
CPF302530253586
CPF3030303586
CPF3535253596

Usable length (cm)

8F9F
Sheath7878
Dilator8383
Loader1012

Sizing recommendations

Distance from defect to aortic root or SVC** (Consider shortest distance)Suggested Cocoon PFO*** device size
Less than 9 mmDo not implant
Between 9 and 12.4 mmCPF18
Between 12.5 and 14.9 mmCPF25
CPF2525
Between 15 and 17.4 mmCPF3025
CPF30
More or equal to 17.5 mmCPF35

Delivery Cable

DescriptionProfile (inch)Length (cm)Catalog Number
6F Delivery Cable0.077117CDC6F

Preclinical Studies

Images from pre-clinical trials of closure device depicting neoendothelialization.Pigs were sacrificed at 36 and 42 days.

Caution

This product is intended for use by or under the direction of a physician. Prior to use, refer to the “Instructions for use” supplied with these devices for indications, contraindications, side effects, suggested procedure warnings and precautions. As part of our continuous product development policy, we reserve the right to change product specifications without prior notification. Information contained herein is for distribution outside the USA & Japan.

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