SEARCH RESULTS FOR: 【溦信88931766】i换脸张子枫11V4G最全所有视频资源全部作品合集.ldb(1724 results)
The Durette® ocular implant, made of clear acrylic material (PMMA), is a smooth-surface motility implant used for enucleation, evisceration, and secondary implantation. There are two 20 mm diameter models that are quasi-spherical: Model I, which has a slightly flattened smooth anterior surface (1 mm flatter vs. a sphere); and Model IV, which has four pronounced mounds (within the sphere) for optimal coupling and motility. The implants have a network of 20 interconnected tunnels (1 to 2 mm) offering the eye surgeon with 3 levels for suturing each rectus muscle, and allowing new tissue to form and integrate with surrounding tissue, while aiming to prevent migration, forward displacement and tissue stretching. They both have an off-center medial posterior elongation for added volume and better front positioning of details for coupling with ocular prostheses.
Oculo-Plastik Inc
12-420
Not in Commercial Distribution
- M8721242003 ()
- Total Volume: 3.5 Milliliter
- Outer Diameter: 20 Millimeter
- Orbital sphere implant
The Durette® ocular implant, made of clear acrylic material (PMMA), is a smooth-surface motility implant used for enucleation, evisceration, and secondary implantation. There are two 20 mm diameter models that are quasi-spherical: Model I, which has a slightly flattened smooth anterior surface (1 mm flatter vs. a sphere); and Model IV, which has four pronounced mounds (within the sphere) for optimal coupling and motility. The implants have a network of 20 interconnected tunnels (1 to 2 mm) offering the eye surgeon with 3 levels for suturing each rectus muscle, and allowing new tissue to form and integrate with surrounding tissue, while aiming to prevent migration, forward displacement and tissue stretching. They both have an off-center medial posterior elongation for added volume and better front positioning of details for coupling with ocular prostheses.
Oculo-Plastik Inc
12-120
Not in Commercial Distribution
- M8721212000 ()
- Total Volume: 4 Milliliter
- Outer Diameter: 20 Millimeter
- Orbital sphere implant
The Reference Plasma Quality Control Kit is for use with the Sonoclot® Analyzer System to verify performance of activated cuvettes. Testing should be performed prior to the use of a new shipment of activated cuvettes and monthly throughout use of the stock. More frequent testing may be required to comply with local, state and federal QC requirements.
Reference plasma quality control is important to properly verify proper performance of coagulation test activators. A two level testing approach is used to perform quality control of the activator used in an activated coagulation test. Level I is run with the activator on the reference plasma. Level II is run with the non-activated test on the reference plasma. These two tests confirm the effectiveness of the activator to perform its intended coagulation activation.
Each Kit contains:
1 vial Reference Plasma Control - 6 ml vial containing a lyophilized preparation of citrated animal plasma, stabilizers and buffer. Contains no human material.
1 vial Distilled Water - 6 ml vial containing 5.0 ml laboratory grade distilled water.
1 vial 0.02 M Calcium Chloride - 6 ml vial containing 5.0 ml 0.02 M Calcium Chloride.
5 plastic 1 ml syringes
2 non-activated test cuvettes (blue with clear caps, stir bars, and probes)
SIENCO, INC.
900-1318
In Commercial Distribution
- B55890013181 ()
900-1318
- Multiple coagulation factor IVD, control
Designed for missions in the most remote and austere environments, the Fresh Whole Blood Transfusion Set contains essential items to collect and transfuse fresh whole blood in a compact sealed package. The set includes a donor module, blood collection bag and recipient module; that allow for donor collection and the ability to perform a transfusion procedure to the recipient.
Product Description
In remote areas and combat environments where definitive care may be too far away or inaccessible, transfusion of fresh whole blood may be the best option for management of hemorrhagic shock in casualties. Blood transfusions have been used successfully in military conflicts and other austere conditions to resuscitate trauma patients suffering from hemorrhagic shock. Developed with extensive research and feedback from the Armed Services Blood Program Office, the Fresh Whole Blood Transfusion Set contains everything needed to test for ABO/Rh compatibility and perform a fresh whole blood transfusion in a compact sealed package.
NOTE: Only personnel trained in blood collection, transfusion, and management of transfusion reactions should use this set.
Combat Capabilities
• Easily administered
• Simplifies training
• Compact lightweight
• Cost effective
Product Attributes
• 100% TAA compliant components (no waivers required)
• Donor and recipient specific modules
• Shelf life: 12 months
• Made in USA
Clinical Benefit
• Assembled in FDA registered facility.
• Adhesive blood bag label for recording donor information.
• EldonCard™: ABO/Rh blood-typing card for simple, accurate, and fast results.
• Re-sealable bag used to send all supplies back with casualty for retrospective testing.
Specifications
• NSN: 6515-01-657-4750
• PN: 80-801
• Single-use
• 12-month Shelf Life
o Does not contain natural rubber latex
• Available Direct and GSA
• 100% TAA Compliant
• Made i
Safeguard US Operating, LLC
1
Not in Commercial Distribution
- M689808010 ()
80-801
- Blood donor set, single-pack
- Blood transfusion set, non-exchange