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SXPD2B425

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SXPD2B425

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Product Name
STRATAFIX™ Spiral PDO Suture
Quick View
Product Category
Wound Closure
Alternative Products
Alternatives Products
SXPD2B424
Additional Specifications
Description
4-0 STRATAFIX SPIRAL PDO VIOLET 14CM X14CM V-26 BIDIRECTIONAL
Brand
STRATAFIX SPIRAL PDO
Suture Size
4-0
Length
6in
Color
VIOLET
Control
NO
Material/Composition
PDO
Category
Wound Closure
Needle Image
QTY/BX
12
Needle Point Type
TAPERCUT
TAPERCUT
Absorbability
ABSORBABLE
Absorption Rate
120-180 DAYS
Directionality
BI-DIRECTIONAL
Pledget
NO
Pledget Size
NA
Needle Name
V-26, V-26
Needle Color
SILVER
Needle Length (mm)
26mm, 26mm
Strands Per Pack
1
Pack Strand/Length
1 x 6in
DISCLAIMER
Do not resterilize. Discard opened, unused STRATAFIX Spiral PDO and associated surgical needles. Users should be familiar with surgical procedure and techniques involving absorbable sutures before employing STRATAFIX Spiral PDO Device for wound closure, as risk of wound dehiscence may vary with the site of application and the suture material used. Physicians should consider the in vivo performance (under ACTIONS section) when selecting a suture for use in patients. The use of this suture may be inappropriate in elderly, malnourished or debilitated patients, or in patients suffering from conditions which may delay wound healing. The safety and effectiveness of STRATAFIX Spiral PDO has been estblished for use in fascial closures (including abdominal wall, thoracic and extremity fascial closures), gastrointestinal surgery or for use in microsurgery, therefore this product should not be used for these purposes. As with any foreign body, prolonged contact of any suture with salt solutions, such as those found in the urinary or biliary tracts may result in calculus formation. As an absorbable suture, STRATAFIX Spiral PDO Device may act transiently as a foreign body. Acceptable surgical practice should be followed for the management of contaminated or infected wounds. As this is an absorbable suture material, the use of supplemental nonabsorbable sutures should be considered by the surgeon in the closure of the sites which may undergo expansion, stretching or distention or which may require additional support. For complete product details, please see Instructions for Use.
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© Ethicon US, LLC. 2017. 085133-171129

For complete indications, contraindications, warnings, precautions, and adverse reactions, please reference full package insert.

This site is published by Ethicon US, LLC, which is solely responsible for its contents, and is intended for U.S. audiences only.

This site is intended for Healthcare Professionals.  If you are a patient, it is important that you discuss information about the benefits and risks of products with your doctor. 

Last updated December 15, 2017. The third-party trademarks used herein are trademarks of their respective owners. Data and usage fees may apply. See your carrier for more information.

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