SEARCH RESULTS FOR: (*Boise State University本科成绩单<网址:ｚｊｗ２１１.ｃｏｍ>白银Natsional*)(2706 results)
BOISE TOTAL HIP-LF
MEDLINE INDUSTRIES, INC.
DYNJ41527M
In Commercial Distribution
- 40198459207014 ()
- 10198459207013 ()
DYNJ41527M
- General surgical procedure kit, non-medicated, single-use
BOISE LAP GASTRIC
MEDLINE INDUSTRIES, INC.
DYNJ902224J
In Commercial Distribution
- 40198459258061 ()
- 10198459258060 ()
DYNJ902224J
- General surgical procedure kit, non-medicated, single-use
BOISE TOTAL KNEE-LF
MEDLINE INDUSTRIES, INC.
DYNJ41528N
In Commercial Distribution
- 40198459279240 ()
- 10198459279249 ()
DYNJ41528N
- General surgical procedure kit, non-medicated, single-use
BOISE TOTAL HIP-LF
MEDLINE INDUSTRIES, INC.
DYNJ41527N
In Commercial Distribution
- 40198459279233 ()
- 10198459279232 ()
DYNJ41527N
- General surgical procedure kit, non-medicated, single-use
BOISE CRANI PACK
MEDLINE INDUSTRIES, INC.
DYNJ50015L
In Commercial Distribution
- 40198459288969 ()
- 10198459288968 ()
DYNJ50015L
- General surgical procedure kit, non-medicated, single-use
BOISE SPINE-LF
MEDLINE INDUSTRIES, INC.
DYNJ41525Q
In Commercial Distribution
- 40198459288952 ()
- 10198459288951 ()
DYNJ41525Q
- General surgical procedure kit, non-medicated, single-use
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
PowerServer is a scalable storage and distribution system for clinical images and data. Images can be stored in lossless or lossy formats. The system is DICOM compliant for image storage, archiving, retrieval, and transmission, and communicates with other DICOM devices. The system also communicates with PowerReader workstations and PowerCache servers. Acquired image data is preserved as captured and changes to display definitions are saved as presentation states so that images may always be reverted back to their initial state. PowerCache is a caching server that communicates with PowerServer and serves PowerReader workstations. A single PowerCache can serve multiple PowerReader workstations, reducing network traffic between PowerReader workstations and PowerServer.
PowerReader is a workstation that views, edits, manipulates, annotates, analyzes, stores, and distributes images and data stored on PowerServer and PowerCache. PowerReader can connect directly to PowerServer and can also connect via PowerCache. PowerReader provides the user with the ability to import, transmit, print, display, store, edit, and process medical images and data.
Gateway is a stand-alone DICOM compliant workstation that views, edits, manipulates, annotates, analyzes, stores, and distributes images and data. Gateway provides the user with the ability to import, transmit, print, display, store, edit, and process medical images and data
Ramsoft Inc
6.0.11.11031A
In Commercial Distribution
- B359PSPACS0 ()
PSPACS6
- Radiology information system
- Radiology information system application software
- Radiology picture archiving and communication system workstation
- Radiological PACS software
The AnovoTM Surgical System is a robotic-assisted device intended for use by laparoscopic trained physicians for endoscopic manipulation of tissue, using graspers and electrosurgery devices during single-site laparoscopic gynecologic procedures such as benign hysterectomy and salpingo-oophorectomy through a transvaginal access point. The system composed of Anovo Surgeon Console, two sterile instruments (Anovo Instrument ARMS), bed-mounted Robotic Control Unit (RCU) and Anovo System Accessories (Unit cables, Sterile Drapes, Robotic Control Unit Support System (RCUSS) and Vaginal Access Kit).
Anovo Surgeon Console (UDI # 07290018151013) packed with its power cable (UDI # 07290018151037)
The Anovo Surgeon Console comprised of Arm Controllers (Joysticks and Thumbsticks), an Adjustable Controllers Stand, a PC with Touch Screen, Manual Release Tool and the Power Adapter, and allowing the operating surgeon to operate the Anovo Instrument Arms. There are two sets of Arm Controllers for the Anovo System: two Thumbsticks and two ARMS Controllers. The ARMS Controllers are enabled only when the system is at “resume” state and allow for the accurate control of the Anovo Instrument ARMS during the surgical procedure. Like the Anovo Instrument Arm, each ARMS Controllers has three joints: wrist, elbow and shoulder, so that each Anovo Instrument ARM moves accordingly to Controller's movement. The surgeon-held Controller handle is above the elbow joint and allows for multiple functionality transitions.
MOMENTIS SURGICAL LTD
-
In Commercial Distribution
- 17290018151027 ()
- Endoscopic electromechanical surgical system
- Electrical mains power cable
Nerivio Infinity is a wireless remote electrical neuromodulation (REN) device for the acute and/or preventive treatment of migraine with or without aura in patients 8 years of age or older. This prescription device is self-applied to the upper arm and should be used in the home environment at the onset of migraine headache or aura. or every other day for preventive treatment. Nerivio Infinity utilizes an endogenous descending analgesic mechanism in which pain in one part of the body inhibits pain in multiple remote body regions (Conditioned Pain Modulation [CPM]).
Nerivio Infinity is a wireless wearable battery-operated device controlled by a mobile software application. The battery is rechargeable, and the electronic unit can be used up to 3 years. The Nerivio Infinity Refill is a disposable and replaceable unit. The refill unit is sufficient for up to 18 treatments of 45 minutes each.
The application has a graphical user interface (GUI) that includes graphical controls that the user can select using a touch screen. This application activates the stimulation, controls the stimulation intensity, monitors the treatment duration, and pauses and terminates the stimulation. The application also provides notifications and indications on the connection state and the remaining number of treatments.
The Nerivio Infinity package under this UDI contains 1 refill unit.
Theranica Bio-Electronics Ltd.
FGD000100
In Commercial Distribution
- 07290017578118 ()
FGD000100
- Craniofacial analgesia electrical stimulator