The Gel Mark UltraCor™ Breast Tissue Marker features a 14G rigid needle with a beveled tip and deploys 4 polylactic acid/polyglycolic acid pellets and one radiopaque marker. The polylactic acid/polyglycolic acid pellets provide approximately 6 weeks of enhanced ultrasound visibility.
Marker Shapes that Celebrate Her
With each purchase of the Heart, Venus or Ring breast tissue marker shapes, BD will contribute $1 to the American Cancer Society™ in honor of breast cancer patients.*
Gel Mark UltraCor™ Breast Tissue Marker PLA/PGA pellets provide approximately 6 weeks of ultrasound enhanced visibility and are essentially resorbed in approximately 12 weeks.
Designed for accuracy and visibility
* Applies to specially marked BD breast tissue marker products purchased from BD. The American Cancer Society™ does not endorse any service or product. Visit bd.com/icoh for details. Valid through September 30.
Please consult product labels and inserts for indications, contraindications, hazards, warnings, precautions and directions for use.
BD-110491
Gel Mark UltraCor™ Breast Tissue Marker
S shape made of Titanium 14G x 10cm
Gel Mark UltraCor™ Breast Tissue Marker
Omega shape made of 316L Stainless Steel 14G x 10cm
BD-19526
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The GelMark UltraCor™ Breast Tissue Marker is intended to radiographically mark breast tissue during a percutaneous biopsy procedure.
This device is not intended for use except as indicated.
1) This device has been designed for single use only. Reusing this medical device bears the risk of cross-patient contamination as medical devices – particularly those with long and small lumina, joints, and/or crevices between components- are difficult or impossible to clean once body fluids or tissues with potential pyrogenic or microbial contamination have had contact with the medical device for an indeterminable period of time. The residue of biological material can promote the contamination of the device with pyrogens or microorganisms which may lead to infectious complications.
2) Do not resterilize. After resterilization, the sterility of the product is not guaranteed because of an indeterminable degree of potential pyrogenic or microbial contamination which may lead to infectious complications. Cleaning, reprocessing and/or resterilization of the present medical device increases the probability that the device will malfunction due to potential adverse effects on components that are influenced by thermal and/or mechanical changes.
3) Patients with a known hypersensitivity to the materials listed in the device description may suffer an allergic reaction to this implant.
4) This device is not recommended for use in patients with breast implants.
5) After use, this product may be a potential biohazard. Handle and dispose of in accordance with acceptable medical practice and applicable local, state, and federal laws and regulations.
6) Avoid the use of excessive force during removal of the Applicator to prevent breakage of the Applicator tip.
7) Do not use in the presence of infection.
1) The device should only be used by physicians trained in percutaneous biopsy procedures.
2) Do not use if the product sterile barrier system or its packaging is compromised.
3) Do not use if Temperature Indicator is black.
4) Ensure all pellets are dispensed.
5) Carefully inspect the device prior to use to verify that device has not been damaged. Do not use if product damage is evident and/or needle is bent.
6) Published studies with comparably sized 316L stainless steel biopsy markers have shown no marker movement and insignificant marker heating when tested in in MRI System with a 1.5T field strength.
Potential complications may include, but are not limited to hematoma, hemorrhage, infection, adjacent tissue injury, pain, allergic reaction, and migration.
