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Nitinol wire used in the Cocoon Septal Occluder is coated with Platinum atoms (up to 25 microns) using nano fusion technology by plasma deposition
*Recapture and redeployment is possible only if delivery cable is securely connected to the disc.
Product Code | Device size (Ø3) (mm) |
Left atrial disc diameter (Ø1) (mm) |
Waist length (L) (mm) |
Right atrial disc diameter (Ø2) (mm) |
Sheath (F) |
---|---|---|---|---|---|
COA08 | 8 | 20 | 3 | 18 | 6-7 |
COA10 | 10 | 22 | 3 | 20 | 6-7 |
COA12 | 12 | 26 | 4 | 22 | 8-9 |
COA14 | 14 | 28 | 4 | 24 | 8-9 |
COA16 | 16 | 30 | 4 | 26 | 8-9 |
COA18 | 18 | 32 | 4 | 28 | 10-12 |
COA20 | 20 | 34 | 4 | 30 | 10-12 |
COA22 | 22 | 36 | 4 | 32 | 10-12 |
COA24 | 24 | 38 | 4 | 34 | 10-12 |
COA26 | 26 | 40 | 4 | 36 | 10-12 |
COA28 | 28 | 42 | 4 | 38 | 10-12 |
COA30 | 30 | 44 | 4 | 40 | 12-14 |
COA32 | 32 | 46 | 4 | 42 | 12-14 |
COA34 | 34 | 50 | 4 | 44 | 12-14 |
COA36 | 36 | 52 | 4 | 46 | 12-14 |
COA38 | 38 | 54 | 4 | 48 | 12-14 |
COA40 | 40 | 56 | 4 | 50 | 12-14 |
COA42 | 42 | 58 | 4 | 52 | 14 |
Usable Length (cm) | |||||||
---|---|---|---|---|---|---|---|
6F | 7F | 8F | 9F | 10F | 12F | 14F | |
Sheath | 60 | 60 | 78 | 78 | 78 | 78 | 78 |
Dilator | 66 | 66 | 84 | 84 | 84 | 84 | 84 |
Loader | 9 | 9 | 9 | 11 | 11 | 13 | 13 |
Description | Profile (inch) | Length (cm) | Catalog Number |
---|---|---|---|
6F Delivery Cable | 0.077 | 117 | CDC6F |
Neoendothelialization on the left atrial surface of the device at 36 days after implantation
Neoendothelialization on the left atrial surface of the device at 42 days after implantation
Neoendothelialization on the right atrial surface of the device at 36 days after implantation
Neoendothelialization on the right atrial surface of the device at 42 days after implantation
References:
1. Hellenic J Cardiol. 2021 Jan 20:S1109-9666(20)30291-8
2. Int J Cardiol. 2014 Dec 15;177(2):418-22.
3. Catheter Cardiovasc Interv. 2015 Sep 1;86(3)
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 U.S. and Japan only.
Check the regulatory status of the device before distribution in areas where CE marking is not the regulation in force. Tests performed by and data on file at Sahajanand Medical Technologies Limited. Illustrations are artist’s representations only and should not be considered as engineering drawings or photographs. Photos on file at Sahajanand Medical Technologies Limited.
Cocoon product range is manufactured by Vascular Innovations Co., Ltd. Thailand, a SMT group company. Cocoon is a trademark of Sahajanand Medical Technologies Limited and its affiliates.
Disclaimer: © Sahajanand Medical Technologies Limited - All rights reserved. Specifications are subject to modification, revision and improvement.