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Description

  • MAXON and MAXON CV synthetic absorbable sutures are prepared from polyglyconate, a copolymer of glycolic acid and trimethylene carbonate
  • MAXON and MAXON CV synthetic absorbable sutures are indicated for use in general soft tissue approximation and/or ligation, including use in pediatric cardiovascular tissue, where growth is expected to occur, and in peripheral vascular surgery
  • MAXON and MAXON CV synthetic absorbable sutures are not indicated for use in adult cardiovascular tissue, ophthalmic surgery, microsurgery and neural tissues
  • MAXON sutures retain approximately 75% of initial tensile strength at two weeks, 65% of at three weeks and 50% at four weeks post-implant
  • Absorption of MAXON sutures is minimal until about 60 days after implant and is essentially complete within six months
  • This product is required to be reported under California Proposition 65

Product Specs

Item Number 250175
Catalog Number 5-516
UOM EA
Level 1 Family Description Nursing and Surgical Supplies
Level 2 Category Description Surgical Instruments
Level 3 Group Description Non-Sterile Surg Instruments
Level 4 Sub-Category Description Bandage Scissors N/S
Application Absorbable Suture with Needle
Brand Maxon
Buy American Act (BAA) Compliant No
Coating Uncoated
Country of Origin Unknown
Manufacturer Covidien
Manufacturer # SMM-5516
McKesson # 501280
Needle 1 Code P-13
Needle Length 13 mm
Needle Length Range 10.1 to 20 mm
Needle Material Alloy Needle
Needle Shape 3/8 Circle
Needle Type Precision Reverse Cutting Needle
Number of Needles 1-Needle
Number of Strands 36-Strand
Sterility Sterile
Suture Color Clear
Suture Length 18 Inch Suture
Suture Length Range 10.1 to 20 in
Suture Material Polyglyconate
Suture Material Range Undyed Synthetic
Suture Size Size 6-0
Suture Type Monofilament
Trade Agreement Act (TAA) Compliant No
UNSPSC Code 42312201

Frequently asked questions

How long does this suture maintain its strength?

The Maxon Polyglyconate suture is engineered for extended tensile strength to support the healing process effectively:

  • At 2 weeks: Retains approximately 75% of its initial strength.
  • At 4 weeks: Retains approximately 50% of its initial strength.
When does the absorption process typically conclude?

This suture offers a highly controlled absorption profile:

  • Minimal absorption occurs until 60 days post-implant.
  • The absorption process is essentially complete within six months.
Is the monofilament design beneficial for tissue passage?

Yes. The monofilament construction is specifically designed to provide:

  • Extremely smooth tissue passage.
  • Minimal drag during placement, which helps reduce trauma to the surgical site.
Is the P-13 needle suitable for delicate procedures?

Absolutely. The P-13 needle is a 13 mm, 3/8 circle precision reverse cutting needle. It is specifically designed to provide high levels of control and precision for delicate soft tissue surgical applications.

What is the suture material composed of?

The suture is made of polyglyconate, which is a specialized copolymer of glycolic acid and trimethylene carbonate. This composition is chosen for its reliable performance in soft tissue approximation.

Are there specific surgical applications for this suture?

This suture is indicated for general soft tissue approximation and/or ligation. This includes specific uses such as pediatric cardiovascular tissue (where growth is expected) and peripheral vascular surgery.

Are there any contraindications for this product?

To ensure patient safety, please note that this suture is not indicated for use in:

  • Adult cardiovascular tissue
  • Ophthalmic surgery
  • Microsurgery
  • Neural tissues
How is the suture provided for clinical use?

The product is provided in a sterile condition to ensure it is ready for immediate clinical use upon opening. Each package contains 36 strands, each measuring 18 inches in length.

Is this product coated for easier handling?

No, this suture is uncoated. The natural properties of the monofilament polyglyconate are utilized to ensure smooth passage through tissue without the need for additional coatings.

What safety disclosures should I be aware of?

This product requires a disclosure under California Proposition 65. Please ensure you are aware of your facility’s requirements for handling products with this specific labeling.