BD-15157 |
Advancing the Open Ventral Hernia Repair Experience
1. Preclinical data on file. Results may not correlate to clinical outcomes.
2. C. R. Bard Inc., bench data on file.
3 Preclinical data on file. Results may not correlate to clinical outcomes.
4 Survey of surgeons attending pre-clinical lab.
Results may not correlate to clinical outcomes. Data on file.
OptiFix™ Open Absorbable Fixation System
Indications
The OptiFix™ Open Absorbable Fixation System is indicated for the fixation of surgical mesh to tissues during open surgical procedures, such as hernia repair.
Contraindications
Contraindications associated with open surgical procedures relative to mesh fixation apply, including but not limited to:
Warnings
The device may not fixate through prosthetics derived from biologic material such as xenografts and allografts. Prosthetic should be evaluated for compatibility prior to use. After use, the OptiFix™ Open Absorbable Fixation System may be a potential biohazard. Handle and dispose of in accordance with any local and federal laws regarding medical waste.
Adverse Reactions
Adverse reactions and potential complications associated with fixation devices such as the OptiFix™ Open Absorbable Fixation System may include, but are not limited to the following: hemorrhage; pain, edema and erythema at wound site; allergic reaction to Poly(D, L)-lactide; infection/septicemia; hernia recurrence/wound dehiscence.
Please consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.
BD-15157 |
1. Preclinical data on file. Results may not correlate to clinical outcomes.
2. C. R. Bard Inc., bench data on file.
3 Preclinical data on file. Results may not correlate to clinical outcomes.
4 Survey of surgeons attending pre-clinical lab.
Results may not correlate to clinical outcomes. Data on file.
OptiFix™ Open Absorbable Fixation System
Indications
The OptiFix™ Open Absorbable Fixation System is indicated for the fixation of surgical mesh to tissues during open surgical procedures, such as hernia repair.
Contraindications
Contraindications associated with open surgical procedures relative to mesh fixation apply, including but not limited to:
Warnings
The device may not fixate through prosthetics derived from biologic material such as xenografts and allografts. Prosthetic should be evaluated for compatibility prior to use. After use, the OptiFix™ Open Absorbable Fixation System may be a potential biohazard. Handle and dispose of in accordance with any local and federal laws regarding medical waste.
Adverse Reactions
Adverse reactions and potential complications associated with fixation devices such as the OptiFix™ Open Absorbable Fixation System may include, but are not limited to the following: hemorrhage; pain, edema and erythema at wound site; allergic reaction to Poly(D, L)-lactide; infection/septicemia; hernia recurrence/wound dehiscence.
Please consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.
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1. Preclinical data on file. Results may not correlate to clinical outcomes.
2. C. R. Bard Inc., bench data on file.
3 Preclinical data on file. Results may not correlate to clinical outcomes.
4 Survey of surgeons attending pre-clinical lab.
Results may not correlate to clinical outcomes. Data on file.
OptiFix™ Open Absorbable Fixation System
Indications
The OptiFix™ Open Absorbable Fixation System is indicated for the fixation of surgical mesh to tissues during open surgical procedures, such as hernia repair.
Contraindications
Contraindications associated with open surgical procedures relative to mesh fixation apply, including but not limited to:
Warnings
The device may not fixate through prosthetics derived from biologic material such as xenografts and allografts. Prosthetic should be evaluated for compatibility prior to use. After use, the OptiFix™ Open Absorbable Fixation System may be a potential biohazard. Handle and dispose of in accordance with any local and federal laws regarding medical waste.
Adverse Reactions
Adverse reactions and potential complications associated with fixation devices such as the OptiFix™ Open Absorbable Fixation System may include, but are not limited to the following: hemorrhage; pain, edema and erythema at wound site; allergic reaction to Poly(D, L)-lactide; infection/septicemia; hernia recurrence/wound dehiscence.
Please consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.