Sale price$1,005.90

Special Order Item

Estimated Delivery:
<p>Earn%20[points_amount]%20when%20completing%20this%20purchase.</p>

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 504615
Catalog Number SMM-5536
UOM BX
Level 1 Family Description Nursing and Surgical Supplies
Level 2 Category Description Wound Closure
Level 3 Group Description Sutures
Level 4 Sub-Category Description Absorbable Sutures, Needled
Application Absorbable Suture with Needle
Brand Maxon
Buy American Act (BAA) Compliant No
Coating Uncoated
Country of Origin Unknown
Manufacturer Covidien
Manufacturer # SMM-5536
McKesson # 504615
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 4-0
Suture Type Monofilament
Trade Agreement Act (TAA) Compliant No
UNSPSC Code 42312201

Frequently asked questions

How long does this suture hold its strength?

The Maxon suture is designed for durable support during critical healing phases. It maintains approximately 75% of its initial strength after two weeks and 50% after four weeks, providing reliable tissue approximation.

Is this suitable for pediatric surgeries?

Yes, this suture is specifically indicated for pediatric cardiovascular applications, among other soft tissue procedures. Its material profile is well-suited for tissues where growth is a factor.

When can I expect complete absorption?

The Maxon suture features a predictable absorption profile: it remains largely intact with minimal absorption until 60 days post-implant, and it achieves essentially complete absorption within six months.

What is the benefit of the reverse cutting needle?

The 3/8 circle precision reverse cutting needle (P-13) is engineered to provide smooth tissue penetration. By utilizing a reverse-cutting configuration, it helps to minimize tissue trauma and tearing during suturing procedures.

Can I use this for ophthalmic or neural surgeries?

No. This suture is not indicated for ophthalmic surgery, microsurgery, neural tissues, or adult cardiovascular tissue. It is strictly intended for general soft tissue approximation and ligation.

What material is this suture made from?

This is a synthetic monofilament suture crafted from polyglyconate, which is a copolymer of glycolic acid and trimethylene carbonate. This material allows for smooth passage through tissues during application.

Is the suture coated for easier handling?

No, this specific suture model is uncoated. Its design relies on the inherent properties of the monofilament polyglyconate to ensure smooth passage through tissue.

What is the size and color of the suture?

This suture is a 4-0 size and is clear in color, providing a minimalist and functional profile for standard surgical procedures.

How should this product be handled?

This suture should be handled in accordance with standard clinical protocols for synthetic, absorbable, monofilament sutures to ensure optimal performance and safety.

Is there a safety warning I should know about?

Yes, this product is required to be reported under California Proposition 65. Please ensure your facility’s compliance protocols account for this requirement.