Mesh, Surgical
Main Filters
Mesh, Surgical
Alafair Biosciences, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
VSC-1 | 0 | - |
AROA BIOSURGERY LIMITED | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
F10243-1017I | 0 | - | ||
F10243-1317I | 0 | - | ||
F10244-1017I | 0 | - | ||
F10244-1520L | 0 | - | ||
F10244-1525L | 0 | - | ||
SR02LG0505US | 0 | - | ||
SR02LG0710US | 0 | - | ||
SR02LG1010US | 0 | - | ||
SR02LG1020US | 0 | - | ||
SR02LG2020US | 0 | - | ||
SR03LG0505US | 0 | - | ||
SR03LG0710US | 0 | - | ||
SR03LG1010US | 0 | - | ||
SR03LG1020US | 0 | - | ||
SR03LG2020US | 0 | - | ||
SR05LG0505US | 0 | - | ||
SR05LG0710US | 0 | - | ||
SR05LG1010US | 0 | - | ||
SR05LG1020US | 0 | - | ||
SR05LG2020US | 0 | - |
Bionova Medical Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
FS1-0505 | 0 | - | ||
FS1-1012 | 0 | - | ||
FS1-1025 | 0 | - | ||
FS1-2025 | 0 | - | ||
FS1-F-0505 | 0 | - | ||
FS1-F-1012 | 0 | - | ||
FS1-F-1025 | 0 | - | ||
FS1-F-2025 | 0 | - |
COOK BIOTECH INCORPORATED | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
C-AFP-0.6X9.5 | 0 | - | ||
C-FP-0.2 | 0 | - | ||
C-FP-0.4 | 0 | - | ||
C-FP-0.7 | 0 | - |
Elutia Med LLC | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
CMCV-124-LRG | 0 | - | ||
CMCV-124-MED | 0 | - |
REPRISE BIOMEDICAL, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
BLM-100-01-0608 | 0 | - | ||
BLM-100-01-0808 | 0 | - | ||
BLM-100-01-0816 | 0 | - | ||
BLM-100-01-1010 | 0 | - | ||
BLM-100-01-1016 | 0 | - | ||
BLM-100-01-1020 | 0 | - |
SYNOVIS LIFE TECHNOLOGIES, INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
PC0404NBIO | 0 | - | ||
PC0404SNBIO | 0 | - | ||
PC0608NBIO | 0 | - | ||
PC0608SNBIO | 0 | - | ||
PC0814NBIO | 0 | - | ||
PC0814SNBIO | 0 | - | ||
PC1016NBIO | 0 | - | ||
PC1016SNBIO | 0 | - | ||
PC1225NBIO | 0 | - |
869 Results
Results Per Page
- 50
- 100
- 250
Catalog #
AvailableQty
Starting At
Name
Company Name
Description
0
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Supple Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
SUPPLE PERI-GUARD Repair Patch is prepared from bovine pericardium cross-linked with glutaraldehyde. The tissue, procured from cattle originating in the USA is chemically sterilized using ethanol and propylene oxide, and treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25°C. SUPPLE PERI-GUARD is MR safe.
0
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Supple Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
SUPPLE PERI-GUARD Repair Patch is prepared from bovine pericardium cross-linked with glutaraldehyde. The tissue, procured from cattle originating in the USA is chemically sterilized using ethanol and propylene oxide, and treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25°C. SUPPLE PERI-GUARD is MR safe.
0
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Supple Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
SUPPLE PERI-GUARD Repair Patch is prepared from bovine pericardium cross-linked with glutaraldehyde. The tissue, procured from cattle originating in the USA is chemically sterilized using ethanol and propylene oxide, and treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25°C. SUPPLE PERI-GUARD is MR safe.
0
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Supple Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
SUPPLE PERI-GUARD Repair Patch is prepared from bovine pericardium cross-linked with glutaraldehyde. The tissue, procured from cattle originating in the USA is chemically sterilized using ethanol and propylene oxide, and treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25°C. SUPPLE PERI-GUARD is MR safe.
0
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Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
Peri-Guard Repair Patch (Peri-Guard) is a biologic tissue prepared from bovine pericardium cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Peri-Guard is chemically sterilized using ethanol and propylene oxide. Peri-Guard is treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C.
0
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Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
Peri-Guard Repair Patch (Peri-Guard) is a biologic tissue prepared from bovine pericardium cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Peri-Guard is chemically sterilized using ethanol and propylene oxide. Peri-Guard is treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C.
0
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Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
Peri-Guard Repair Patch (Peri-Guard) is a biologic tissue prepared from bovine pericardium cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Peri-Guard is chemically sterilized using ethanol and propylene oxide. Peri-Guard is treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C.
0
-
Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
Peri-Guard Repair Patch (Peri-Guard) is a biologic tissue prepared from bovine pericardium cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Peri-Guard is chemically sterilized using ethanol and propylene oxide. Peri-Guard is treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C.
0
-
Peri-Guard
SYNOVIS LIFE TECHNOLOGIES, INC.
Peri-Guard Repair Patch (Peri-Guard) is a biologic tissue prepared from bovine pericardium cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Peri-Guard is chemically sterilized using ethanol and propylene oxide. Peri-Guard is treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C.
0
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VersaWrap
Alafair Biosciences, Inc.
The VersaWrap wetting Solution is applied to the Sheet to render the Sheet a gelatinous, tissue adherent layer (gel in situ). The aqueous citrate Solution is provided sterile, non-pyrogenic, for single use, in a dropper, packaged in a double peel pouch.
0
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OviTex IHR Reinforced Bioscaffold with Permanent Polymer (bean)
AROA BIOSURGERY LIMITED
The OviTex® Reinforced Tissue Matrix Device is a sterile reinforced matrix device comprised of non-dermal sourced layers of extracellular matrix (ECM) (ovine (sheep) derived ECM), paired with a minimal suture footprint. OviTex Reinforced Tissue Matrix Device provides an alternative device solution to permanent synthetic, resorbable/bioabsorbable synthetic, and biologic meshes. The device remodels and helps regenerate tissue while reinforcing the repair and providing structural support. Reinforced tissue matrices enhance performance while maintaining compatibility with the body. The OviTex Reinforced Tissue Matrix Device is used for inguinal hernia repair.
0
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OviTex IHR Reinforced Bioscaffold with Permanent Polymer (bean)
AROA BIOSURGERY LIMITED
The OviTex® Reinforced Tissue Matrix Device is a sterile reinforced matrix device comprised of non-dermal sourced layers of extracellular matrix (ECM) (ovine (sheep) derived ECM), paired with a minimal suture footprint. OviTex Reinforced Tissue Matrix Device provides an alternative device solution to permanent synthetic, resorbable/bioabsorbable synthetic, and biologic meshes. The device remodels and helps regenerate tissue while reinforcing the repair and providing structural support. Reinforced tissue matrices enhance performance while maintaining compatibility with the body. The OviTex Reinforced Tissue Matrix Device is used for inguinal hernia repair.
0
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OviTex IHR Reinforced Bioscaffold with Permanent Polymer (bean)
AROA BIOSURGERY LIMITED
The OviTex® Reinforced Tissue Matrix Device is a sterile reinforced matrix device comprised of non-dermal sourced layers of extracellular matrix (ECM) (ovine (sheep) derived ECM), paired with a minimal suture footprint. OviTex Reinforced Tissue Matrix Device provides an alternative device solution to permanent synthetic, resorbable/bioabsorbable synthetic, and biologic meshes. The device remodels and helps regenerate tissue while reinforcing the repair and providing structural support. Reinforced tissue matrices enhance performance while maintaining compatibility with the body. The OviTex Reinforced Tissue Matrix Device is used for inguinal hernia repair.
0
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OviTex LPR Reinforced Bioscaffold
AROA BIOSURGERY LIMITED
The OviTex® Reinforced Tissue Matrix Device is a sterile reinforced matrix device comprised of non-dermal sourced layers of extracellular matrix (ECM) (ovine (sheep) derived ECM), paired with a minimal suture footprint. OviTex Reinforced Tissue Matrix Device provides an alternative device solution to permanent synthetic, resorbable/bioabsorbable synthetic, and biologic meshes. The device remodels and helps regenerate tissue while reinforcing the repair and providing structural support. Reinforced tissue matrices enhance performance while maintaining compatibility with the body. The OviTex Reinforced Tissue Matrix Device is used for hernia repair and abdominal wall reconstruction.
0
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OviTex LPR Reinforced Bioscaffold
AROA BIOSURGERY LIMITED
The OviTex® Reinforced Tissue Matrix Device is a sterile reinforced matrix device comprised of non-dermal sourced layers of extracellular matrix (ECM) (ovine (sheep) derived ECM), paired with a minimal suture footprint. OviTex Reinforced Tissue Matrix Device provides an alternative device solution to permanent synthetic, resorbable/bioabsorbable synthetic, and biologic meshes. The device remodels and helps regenerate tissue while reinforcing the repair and providing structural support. Reinforced tissue matrices enhance performance while maintaining compatibility with the body. The OviTex Reinforced Tissue Matrix Device is used for hernia repair and abdominal wall reconstruction.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
-
Myriad Matrix Soft Tissue Bioscaffold
AROA BIOSURGERY LIMITED
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
0
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EluPro Antibiotic-Eluting BioEnvelope
Elutia Med LLC
The EluPro Antibiotic-Eluting BioEnvelope is a sterile pouch designed to hold a cardiac implantable device or implantable neurostimulator device to create a stable environment when implanted in the body. EluPro consists of decellularized, non-crosslinked, lyophilized extracellular matrix (ECM) and resorbable, ring- shaped poly(D,L Lactide-Co-Glycolide) (PLGA) discs containing the antibiotics rifampin and minocycline. The ECM material is derived from porcine small intestinal submucosa (SIS). The envelope is constructed with four multilaminate sheets, perforated to allow for the natural flow of exudate through the device. The drug-eluting polymer discs are secured between the multilaminate sheets on each side and the envelope is constructed with 5-0 polydioxanone (PDS) suture. EluPro contains 10.5 mg of rifampin and 9.3 mg of minocycline.
0
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EluPro Antibiotic-Eluting BioEnvelope
Elutia Med LLC
The EluPro Antibiotic-Eluting BioEnvelope is a sterile pouch designed to hold a cardiac implantable device or implantable neurostimulator device to create a stable environment when implanted in the body. EluPro consists of decellularized, non-crosslinked, lyophilized extracellular matrix (ECM) and resorbable, ring- shaped poly(D,L Lactide-Co-Glycolide) (PLGA) discs containing the antibiotics rifampin and minocycline. The ECM material is derived from porcine small intestinal submucosa (SIS). The envelope is constructed with four multilaminate sheets, perforated to allow for the natural flow of exudate through the device. The drug-eluting polymer discs are secured between the multilaminate sheets on each side and the envelope is constructed with 5-0 polydioxanone (PDS) suture. EluPro contains 10.5 mg of rifampin and 9.3 mg of minocycline.