Dolphin Sutures

Durafibr · Non-Absorbable Sutures

UHMWPE Sutures

DURAFIBR is a sterile, non-absorbable braided UHMWPE suture with polyester, undyed with a blue tracer, engineered for high tensile strength and durable handling in orthopaedic and heavy-tissue surgical closure.

ISO 13485MDSAPSterile, single use
UHMWPE Sutures
UHMWPE Sutures

01

Braided UHMWPE construction

Composed of medical-grade ultra-high-molecular-weight polyethylene with polyester, giving a strong, flexible, abrasion-resistant braid suited to demanding soft- and hard-tissue closure.

02

High tensile strength

The long-chain linear polyethylene provides high tensile and flexural strength, supporting durable approximation and ligation where prolonged mechanical support is required.

03

Blue tracer visibility

Supplied undyed with a blue tracer woven into the braid, improving intraoperative visibility of the suture within the surgical field.

04

Central core backbone

A sturdy core running through the centre of the braid acts as a backbone, supporting knot tying and consistent handling characteristics during placement.

05

Non-absorbable support

As a non-absorbable material, DURAFIBR is not absorbed by the body and maintains mechanical support over the long term for procedures needing prolonged retention.

06

Low-friction handling

A low coefficient of friction and lubricious braid allow each knot to slide smoothly, supporting efficient knot placement with corrosion resistance.

What DURAFIBR UHMWPE Suture Is

DURAFIBR is a sterile, non-absorbable, braided surgical suture composed of ultra-high-molecular-weight polyethylene (UHMWPE) with polyester. It is intended for general soft and hard tissue approximation and ligation wherever a non-absorbable suture is indicated. Because the material is not absorbed by the body, it is well suited to procedures requiring prolonged mechanical support, including orthopaedic, arthroscopic, shoulder, rotator cuff, knee, and ankle repairs.

Composition and Construction

The suture is built from braided UHMWPE combined with polyester, a long-chain linear polyethylene that enables high tensile and flexural strength for demanding wound closure. DURAFIBR is supplied undyed with a blue tracer for improved intraoperative visibility. A sturdy central core runs through the braid to act as a backbone, supporting knot tying and consistent handling. The construction delivers corrosion resistance and a low coefficient of friction.

Characteristics and Handling

DURAFIBR is a flexible, strong, abrasion-resistant suture with a lubricious braid that allows each knot to slide for smoother placement. Its combination of UHMWPE and polyester is intended to provide high tensile strength, durability, and reliable handling. The suture elicits minimal initial inflammatory tissue reaction and, being non-absorbable, maintains mechanical support over the long term. Standard flat, square ties with additional throws as clinically indicated help secure knots.

Presentations

DURAFIBR is available in gauge sizes 2-0, 2, and 5, in undyed and co-dyed versions, with or without permanently attached surgical needles of varying types and shapes. Needle options include 1/2 circle taper-cutting and cutting profiles at 23 mm and 37 mm needle lengths, with 90 cm suture lengths.

General SurgeryOrthopaedic Surgery

Frequently Asked Questions

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What is DURAFIBR made of?
DURAFIBR is a braided surgical suture composed of ultra-high-molecular-weight polyethylene (UHMWPE) with polyester. It is supplied undyed with a blue tracer, in undyed and co-dyed versions, with or without permanently attached surgical needles.
What is DURAFIBR intended for?
It is intended for general soft and hard tissue approximation and ligation where a non-absorbable suture is indicated, including orthopaedic, arthroscopic, shoulder, rotator cuff, knee, and ankle procedures, and other heavy tissue approximation as determined appropriate by the surgeon.
Is DURAFIBR absorbable?
No. DURAFIBR is a non-absorbable suture and is not intended to be absorbed by the body. Because it is non-absorbable, it maintains mechanical support over the long term, making it suitable for procedures requiring prolonged tissue support.
What sizes and needle options are available?
DURAFIBR is available in gauge sizes 2-0, 2, and 5. Needle options include 1/2 circle taper-cutting and cutting profiles at 23 mm and 37 mm needle lengths, supplied in 90 cm suture lengths, with or without permanently attached needles.
Is DURAFIBR supplied sterile?
Yes. DURAFIBR is supplied sterile and is sterilized by ethylene oxide (EO). It is a single-use device and must not be reused, reprocessed, or resterilized. Do not use if the package is opened, damaged, or compromised.
How should DURAFIBR be stored?
Store at 10°C to 35°C, away from moisture and direct heat, and protect from direct sunlight. Do not use after the expiry date. The shelf life is five years from the date of manufacture or sterilization, subject to package integrity and the labeled expiry date.
Who should use DURAFIBR?
DURAFIBR is intended for qualified surgeons and trained healthcare professionals familiar with non-absorbable sutures and the relevant surgical techniques. Surgeons should be familiar with procedures involving non-absorbable sutures before use, as wound dehiscence risk may vary by application site.
How can distributors obtain documentation and ordering details?
Distributors and procurement teams can contact Dolphin Sutures for product codes, available size and needle configurations, the Instructions for Use, and regulatory documentation to support registration, tendering, and ordering across international markets.

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