202050
Integra DuraSeal Cranial Sealant System 5ml
$799.00
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Description
Integra DuraSeal Cranial Sealant System
The hydrogel technology of the DuraSeal® Family of products offers sealing solutions to reinforce CSF leakages prevention during dural repair procedures.
Product Code: 202050
- Burst Strength: DuraSeal® system offers features tissue adherence and cohesive strength to withstand critical CSF pressures during cranial procedures.
- Biocompatibility: DuraSeal® system is made from polyethylene glycol hydrogel (100% synthetic inert materiel).
- Resorption: the DuraSeal® hydrogel is resorbed after 4 to 8 weeks, providing enough time for dura to heal adequately following application.
- Blue colorant: provides visualization and allows to assess sealant coverage and thickness
- Tight Spaces: the flexible and non-clogging applicators compatible with the DuraSeal® system allows to access to hard-to-reach areas of the brain.
Additional Details
- Company Name: Integra Lifesciences Corporation
- FDA Product Code: NQR
- FDA Product Code Name: Sealant, Dural
- GMDN Term Code: 47171
- GMDN Term Name: Dura mater sealant
- GMDN Term Definition: An implanted bioabsorbable material (e.g., solution, gel, spray, patch) intended to be applied to a defect in the dura mater, possibly as an adjunct to standard methods of closure (e.g., suturing), to prevent cerebrospinal fluid (CSF) leakage during healing. The material primarily consists of synthetic polymers that subsequently form adhesive bonds with the dura mater and eventually degrade and are absorbed. After application, this device cannot be reused.
Additional information
| Size | 1 |
|---|---|
| Arms | N/A |
| Manufacturer | |
| Unit | eaches |
- FDA Product Code: NQR
- FDA Product Code Name: Sealant, Dural
- GMDN Term Code: 47171
- GMDN Term Name: Dura mater sealant
- GMDN Term Description: An implanted bioabsorbable material (e.g., solution, gel, spray, patch) intended to be applied to a defect in the dura mater, possibly as an adjunct to standard methods of closure (e.g., suturing), to prevent cerebrospinal fluid (CSF) leakage during healing. The material primarily consists of synthetic polymers that subsequently form adhesive bonds with the dura mater and eventually degrade and are absorbed. After application, this device cannot be reused.
