Hypro-Sorb F® Membrane
Hypro-Sorb® F is a rigid, bilayer membrane made of 99.9% pure, crystalline Atelo-Collagen Type I, which is derived from the bovine Achilles tendon. Hypro-Sorb® F is 0.2 mm thick with high tensile and bending strength due to densely packed collagen fibers. Therefore, it is recommended to soak the membrane with saline or the patient’s blood for at least 1 minute before application to facilitate handling.

The resorption process occurs in two phases. During the first six to eight weeks,
Hypro-Sorb® F stays intact. The resorption of the membrane starts afterwards. The membrane is completely resorbed within six months.

PROPERTIES AND ADVANTAGES
0.2 mm rigid, bilayer membrane

pure, crystalline Atelo-Collagen Type I, free of immunogenic telopeptides

highest degree of tissue biocompatibility

highest safety with excellent wound healing characteristics

quick adaptation to the defect due to it is potent hydrophilic properties

reduced risk of dehiscence formation due to the texture and mild bacteriostatic effect of Atelo-Collagen

long barrier function of circa 16 weeks, complete resorption after 6 months

rough and smooth sides are clearly distinguishable

sterile and safe for five years after production

Hypro-Sorb® F membrane
Hypro-Sorb® F is a rigid, two-layer membrane made from 99.9% pure, crystalline atelo-collagen type I, which is obtained from the bovine Achilles tendon. Hypro-Sorb® F is 0.2 mm thick and has particularly high tensile and flexural strength due to densely packed collagen fibers. Therefore, for ease of use, we recommend soaking the membrane in saline or blood for at least 1 minute prior to use.

Membrane absorption occurs in two phases. Stays during the first six to eight weeks

Hypro-Sorb® F completely intact. The degradation process only begins after this time. The membrane is completely resorbed after six months.

FEATURES AND BENEFITS
0.2 mm rigid, two-layer membrane

pure, crystalline atelo-collagen type I, free from antigenic telopeptides

highest level of tissue biocompatibility

highest safety with excellent wound healing properties

rapid adaptation to the wound due to strong hydrophilic properties

reduced risk of dehiscence formation due to the stable consistency and bacteriostatic effect of atelo-collagen

long barrier function of around 16 weeks, complete resorption after 6 months

rough and smooth side of the membrane are clearly distinguishable

sterile and safe for five years from the date of manufacture

Perfect handling
No mixing – use directly from the syringe.
Ergonomic syringe for direct application through the osteotomy or small sinus window.
Easily moulded to match defect morphology.
Resilience to wash-away – even in a wet field.
No membrane
Perfect stability and resilience to micromovement – ideal for minimal access approaches with site-specific flap.
Premium Performance
‘significantly enhanced bone regeneration compared to β-TCP.’ (3,4)
‘radiographically, and histologically equivalence to autograft. (7)
Powerbone Putty resorbs completely in line with bone healing making it perfect for:
Socket grafting.
3 walled GBR defects.
Sinus Lift.
Bony Cysts.

TITANIUM PIN (Grade 5)SET

The ergonomic design of the applicator allows easy removal of the pin and easy
fixation of the membrane.The notch, which is approximately half the length of the
pin, ensures that the pin is pin engages bone easily.
Ergonomically designed for easy capture and quick application of titanium pins. The Pin Applicator offers single-handed fixation of resorbable and non-resorbable membranes.

The macro geometry of The macro geometry of Titanium Pins head allows
insertion without bone preparation whilst the head design prevents bending during
application. These features result in higher torque insertion, better primary stability,
and a more predictable success rate.
Distortion of the pin apex during handling
cannot occur.

PROPERTIES
TITANIUM PIN (Grade 5)SET
The ergonomic design of the applicator allows easy removal of the pin and easy
fixation of the membrane. The notch, which is approximately half the length of the
pin, ensures that the pin is pin engages bone easily.

Ergonomically designed for easy capture and quick application of titanium pins. The Pin Applicator offers single-handed fixation of resorbable and non-resorbable membranes.

The macro geometry of The macro geometry of Titanium Pins head allows
insertion without bone preparation whilst the head design prevents bending during
application. These features result in higher torque insertion, better primary stability,
and a more predictable success rate.

cannot occur.

• Ligamed Flexible Strip Implantation;
• Ligamed Flexible Strip can be applied to the
surgical area directly or combined with bone marrow
aspirate or blood.
• When the Ligamed Flexible Strip is wetted with
blood, its flexibility increases significantly.
• Ligamed Flexible Strip must be implanted just
before all metallic implants are stabilized and the
surgical site is closed.
• Ligamed Flexible Strip can be cut and placed in
the spinal cage.
• Ligamed Flexible Strip gains osteoinductive
characteristic due to silicate addition to the product
content.

SILICATE ADDITIVE GRANULE, STICK & BLOCK Safe, Biocompatible and Sterile Ligamed grafts are supplied sterile and is CE marked as a Class III Medical Device according to 93/42 / EC medical device directive. Biocompatibility tests (in vitro and in vivo), biodegradation tests, bioburden and sterility tests were applied to the products.

Radiopaque CT and X-ray traceability is possible. 100% Synthetic Does not contain human or animal tissue,therefore there is no risk of disease transmission. 0.25-9 mm.

Osteoconductive and Osteoinductive It supports new bone formation. It acts as a roof for the cells that enable new bone formation. It has a structure similar to the mineral found naturally in bone. The silicate additive increases the protein retention to the graft and gives it bioactive characteristics.

Ligamed products are designed to repair bone defects caused
by surgery or traumatic injury, increase bone formation or
support the formation of new bone tissue in non-load bearing
clinical applications. It can be mixed with bone marrow, blood
and other clinically known bone grafts.

Ligamed products are designed to repair bone defects caused
by surgery or traumatic injury, increase bone formation or
support the formation of new bone tissue in non-load bearing
clinical applications. It can be mixed with bone marrow, blood
and other clinically known bone grafts.

Ligamed products are designed to repair bone defects caused by surgery or traumatic injury, increase bone formation or support the formation of new bone tissue in non-load bearing clinical applications. It can be mixed with bone marrow, blood and other clinically known bone grafts.

Ligamed products are designed to repair bone defects caused
by surgery or traumatic injury, increase bone formation or
support the formation of new bone tissue in non-load bearing
clinical applications. It can be mixed with bone marrow, blood
and other clinically known bone grafts.

cerabone® plus combines the established bovine bone grafting material cerabone® with the well-known properties of hyaluronic acid. Thanks to the pronounced liquid binding capacities of hyaluronate, cerabone® plus forms a sticky bone material upon hydration that provides unique application comfort by allowing both easy uptake and delivery to the site of application.

cerabone® plus combines the established bovine bone grafting material cerabone® with the well-known properties of hyaluronic acid. Thanks to the pronounced liquid binding capacities of hyaluronate, cerabone® plus forms a sticky bone material upon hydration that provides unique application comfort by allowing both easy uptake and delivery to the site of application.