Interceed Medical Device

GYNECARE INTERCEED® Adhesion Prevention | Ethicon - J&J …

https://www.jnjmedtech.com/en-US/product/gynecare-interceed-absorbable-adhesion-prevention-barrier

GYNECARE INTERCEED ® Absorbable Adhesion Barrier Provides an extra layer of assurance against the risk of adhesions. It does not crack, tear, or stick to gloves. It’s pliability allows it to contour to organs of varying sizes for full coverage. Request …

Adhesion barrier - Wikipedia

https://en.wikipedia.org/wiki/Adhesion_barrier

Uterine & Pelvic | Ethicon - J&J MedTech

https://www.jnjmedtech.com/en-US/product-family/uterine-pelvic-original

The safety and effectiveness of using GYNECARE INTERCEED ® in combination with other adhesion prevention treatments have not been clinically established. GYNECARE …

Premarket Approval (PMA) - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P880047S047

GYNECARE INTERCEED™ Absorbable Adhesion Barrier: Generic Name: barrier, absorbable, adhesion: Applicant: ETHICON, INC. 1000 route 202 raritan, NJ 08869: PMA …

Gynecare Interceed® Adhesion Barrier - Normedi Nordic

https://normedi.com/products/laparoscopy/adhesion-prevention/gynecare-interceed-adhesion-barrier/

Gynecare Interceed® Adhesion Barrier. GYNECARE INTERCEED® Adhesion Barrier has been proven to reduce the formation of pelvic adhesions to provide you with control …

AccessGUDID - DEVICE: GYNECARE INTERCEED …

https://accessgudid.nlm.nih.gov/devices/10705031005396

GMDN Definition. Surgical anti-adhesion material, implantable, bioabsorbable, non-medicated. A bioabsorbable, surgically-implanted device intended to …

4350 | Ethicon

https://www.ethicon.com/na/epc/code/4350

Before using any medical device, review all relevant package inserts with particular attention to the indications, contraindications, warnings and …

Resorbable Adhesion Barrier Devices for Use in …

https://www.fda.gov/regulatory-information/search-fda-guidance-documents/guidance-resorbable-adhesion-barrier-devices-use-abdominal-andor-pelvic-surgery-guidance-industry

Clinical evaluation of significant risk devices requires an approved Investigational Device Exemption (IDE) application in addition to IRB approval. The FD&C Act authorizes the …

Premarket Approval (PMA) - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P880047

The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling …

Intercede Health

https://intercedehealth.com/

Founded in 1995, Intercede Health has decades of experience working with its partners in the management of complex health conditions. We are focused on …