SEARCH RESULTS FOR: (*One Satoshitg:(@hkotccc)tFIg*)(1754743 results)
Only the first 10,000 results were returned. Filter these results or refine your query. Some pre-built queries with more than 10,000 results are available for download.
No Description
Ellis Instruments Inc
#125-080
In Commercial Distribution
- 00860007290640 ()
- Surgical implant handling forceps
No Description
Ellis Instruments Inc
#125-025
In Commercial Distribution
- 00860007290626 ()
- Surgical implant handling forceps
No Description
Ellis Instruments Inc
#125-024
In Commercial Distribution
- 00860007290602 ()
- Surgical implant handling forceps
Canvas Dx is a prescription diagnostic aid to healthcare professionals (HCP) considering the diagnosis of Autism Spectrum Disorder (ASD) in patients 18 months through 72 months of age at risk for developmental delay. The patient’s caregiver uses a smartphone application (“App”) to fill out a caregiver questionnaire and to make video recordings of behavior at home, and then the physician fills out a medical questionnaire online. The results are made available to the physician.
Cognoa, Inc.
1.3.0
In Commercial Distribution
- 00860007260605 ()
- Neurodevelopmental disorder interpretive software
Oscillating Saw Packaged Assembly
Insurgical, Inc.
320-0067-001
In Commercial Distribution
- 00860007230035 ()
3010002
- Bone/joint surgical power tool motorized handpiece/set, electric, single-use
Reciprocating Saw Packaged Assembly
Insurgical, Inc.
320-0071-001
In Commercial Distribution
- 00860007230028 ()
3010003
- Bone/joint surgical power tool motorized handpiece/set, electric, single-use
Drill-Reamer Packaged Assembly
Insurgical, Inc.
320-0064-001
In Commercial Distribution
- 00860007230004 ()
3010001
- Bone/joint surgical power tool motorized handpiece/set, electric, single-use
The NeuraMedica Instrument Tray is a separately-supplied reusable surgical tray that holds the instrument that aids in the installation of the NeuraMedica Durafuse Dural Clips.
Neuramedica Inc.
TR-200
In Commercial Distribution
- 00860007130434 ()
- Instrument tray, reusable
The NeuraMedica Instrument Tray is a separately-supplied reusable surgical tray that holds the instrument that aids in the installation of the NeuraMedica Durafuse Dural Clips.
Neuramedica Inc.
TR-100
In Commercial Distribution
- 00860007130427 ()
- Instrument tray, reusable
NeuraMedica Dural Clips are bioabsorbable surgical clips designed to aid in closure of the dura mater in neurosurgical and orthopedic spine procedures. NeuraMedica Dural Clips are 3mm wide by 4.6mm long. They are applied using a reusable stainless steel applier. The NeuraMedica Applier is a separately-supplied reusable instrument.
Neuramedica Inc.
DC-501
In Commercial Distribution
- 00860007130403 ()
- Ligation clip, synthetic polymer, bioabsorbable
Accessory connector to be used with Venturi MicroDry, compatible with Olympus endoscope
GI Scientific LLC
Universal Connector with Auxiliary Jet Connector Olympus
In Commercial Distribution
- 00860007020926 ()
VDU-06-00023
- Surgical instrument/endoscope cleaning utensil, reusable
No Description
Precision For Medicine, Inc.
001
In Commercial Distribution
- 00860006973520 ()
- General specimen collection kit IVD, clinical
Coolject Standard Nozzle Accessory, One per Box
Vapocoolshot, Inc
VM01100-00
In Commercial Distribution
- 00860006961558 ()
- Cold/cool therapy spray
Coolject 1-3 cc Syringe Holder Nozzle Accessory, One per Box
Vapocoolshot, Inc
VM01000-00
In Commercial Distribution
- 00860006961534 ()
- Biopsy syringe holder, reusable
The Prosidio L.E. all-in-one camera system is an all-in-one camera system for rigid and flexible endoscopes.
Prosidio LLC
L.E. All-in-one endoscopy system V1.0
In Commercial Distribution
- 00860006918705 ()
LE001
- Endoscopic video image processing/light source system
- Endoscope video camera
Medical Ultraviolet Air Purifier
ACTIVEPURE MEDICAL LLC
F170A
In Commercial Distribution
- 00860006810108 ()
- High-efficiency filter air cleaner, mobile
Three Pack Nosebleed Tourniquet Device - Small, Medium, Large (00860006794705, 00860006794712, 00860006794729)
Product Motif Inc.
01-PN-020
In Commercial Distribution
- 00860006794767 ()
01-PN-020
- Intranasal splint, non-biodegradable
Single Pack Nosebleed Tourniquet Device - Large
Product Motif Inc.
01-PN-016
In Commercial Distribution
- 00860006794729 ()
- 00860006794750 ()
01-PN-016
- Intranasal splint, non-biodegradable
Single Pack Nosebleed Tourniquet Device - Medium
Product Motif Inc.
01-PN-015
In Commercial Distribution
- 00860006794712 ()
- 00860006794743 ()
01-PN-015
- Intranasal splint, non-biodegradable
Single Pack Nosebleed Tourniquet Device - Small
Product Motif Inc.
01-PN-014
In Commercial Distribution
- 00860006794705 ()
- 00860006794736 ()
01-PN-014
- Intranasal splint, non-biodegradable
Regulated Software Application (RSA), Version 2.0 is a stand-alone blood establishment computer software application (BECS) that provides management controls and information services that have been designed to assist personnel in the operation of a blood center.
ARC-ONE SOLUTIONS, LLC
2.0.0.0
In Commercial Distribution
- 00860006793708 ()
2.0.0.0
- Blood bank information system application software
No Description
Lgc Clinical Diagnostics, Inc.
2000-0100
In Commercial Distribution
- 00860006589783 ()
- Multiple blood-borne virus antigen/antibody IVD, control
No Description
Lgc Clinical Diagnostics, Inc.
2000-0079
In Commercial Distribution
- 00860006589776 ()
- Multiple blood-borne virus antigen/antibody IVD, control
No Description
Lgc Clinical Diagnostics, Inc.
2000-0080
In Commercial Distribution
- 00860006589707 ()
- Multiple blood-borne virus antigen/antibody IVD, control
Gro3X DIU system is an optical impression system used to record the topographical characteristics of teeth, dental impressions, or stone models for use in the computer aided design and manufacturing of dental restorative prosthetic devices. Gro3X DIU system consists of a handheld scanner with base, tips (reusable upon autoclave), cables and software.
Gro3x, Inc.
DIU-3D-71-001
In Commercial Distribution
- 00860006572501 ()
- Dental milling system, CAD/CAM, chairside
Rapid Acoustic Pulse Device (RAP) is designed as an accessory to laser treatments to improve laser tattoo fading efficiency, as well as a stand alone device to improve the appearance of cellulite.
Soliton Inc
Rapid Acoustic Pulse Device (RAP) GEN-2.2
In Commercial Distribution
- 00860006515102 ()
1004900-MDC-003
- General/multiple surgical diode laser system
No Description
Aerus LLC
F170A
In Commercial Distribution
- 00860006514808 ()
- High-efficiency filter air cleaner, mobile
The HMS-1000 hyperbaric chamber series is a Class B, monoplace hyperbaric chamber designed to treat one (1) patient to a maximum operating pressure of three (3) Atmospheres Absolute (ATA) (~ 29.4 psi). The chamber uses 100% oxygen as both the pressurization and hyperbaric treatment gas. The overall external length of the horizontal cylinder configuration is 8.75 feet. Its internal diameter is 33.5 inches. It is constructed of acrylic, aluminum, and fine-grade steel. Single operator pressure control is achieved via a simple industrial Programmable Logic Device (PLD) controller. A low-voltage patient intercom provides communications between the patient in the chamber and the external chamber operators. HMS-1000 is designed, fabricated, and tested in compliance with the following FDA consensus standards: the American Society of Mechanical Engineers / Pressure Vessel for Human Occupancy (ASME/PVHO-1) and the National Fire Protection Agency (NFPA) 99, Health Care Facilities.
Hyperbaric Modular Systems Inc.
HMS-1000
In Commercial Distribution
- 00860006478964 ()
- Hyperbaric chamber, stationary
The HMS-2000 is a Class A, single compartment pressure vessel for human occupancy (PVHO) that is oriented in a vertical cylindrical geometry. The HMS-2000 hyperbaric chamber family of products is designed with non-dedicated seating, providing flexibility in managing seating arrangements. The diameter of the HMS-2000 varies in size; thereby enabling the ability to increase the patient capacity from three (3) to four (4) seated patients. An extension nozzle is attached to the chamber hull which provides the unique capability to treat one (1) patient in the supine versus seated position. The maximum allowable working pressure is three (3) Atmospheres Absolute (ATA) (~29.4psi). The control and operation of the HMS-2000 is performed from a hull mounted control console. The HMS-2000 multiplace hyperbaric chamber is designed, fabricated, and tested in compliance with the following FDA consensus standards: the American Society of Mechanical Engineers / Pressure Vessel for Human Occupancy (ASME/PVHO-1) and the National Fire Protection Agency (NFPA) 99, Health Care Facilities.
Hyperbaric Modular Systems Inc.
HMS-2000
In Commercial Distribution
- 00860006478940 ()
- Hyperbaric chamber, stationary
The HMS-4000 is a Class A, pressure vessel for human occupancy (PVHO) that is designed in a horizontal cylindrical geometry. Configurations vary from one (1) to three (3) compartments. These chambers are capable of administering hyperbaric oxygen therapy treatments to four (4) up to twenty-four (24) patients simultaneously. These chamber models comprise the HMS 4000 Horizontal Cylindrical Multiplace Hyperbaric Chamber System Product Family. Each system consists of a multiplace hyperbaric chamber with several major subsystems that are interconnected to form a complete system, which includes an operation control system that uses computer control technology. Design pressures range from 3ATA (~29.4psi) up to 6ATA (~73.5psi). The HMS-4000 multiplace hyperbaric chamber is designed, fabricated, and tested in compliance with the following FDA consensus standards: American Society of Mechanical Engineers / Pressure Vessel for Human Occupancy (ASME/PVHO-1) and the National Fire Protection Agency (NFPA) 99, Health Care Facilities.
Hyperbaric Modular Systems Inc.
HMS-4000
In Commercial Distribution
- 00860006478926 ()
- Hyperbaric chamber, stationary
The HMS-5000-12 is a Class A, pressure vessel for human occupancy (PVHO) that is designed in a rectangular geometry. It has two (2) compartments and is capable of administering hyperbaric oxygen therapy treatments up to twelve (12) patients simultaneously. It is one of the models contained within the HMS 5000 Rectangular Multiplace Hyperbaric Chamber System Product Family. It is comprised of a multiplace hyperbaric chamber with a number of major subsystems that are interconnected to form a complete system, which includes an operation control system that uses computer control technology. Pressures up to 6ATA (~73.5psi). The HMS-5000 multiplace hyperbaric chamber is designed, fabricated, and tested in compliance with the following FDA consensus standards: American Society of Mechanical Engineers / Pressure Vessel for Human Occupancy (ASME/PVHO-1) and the National Fire Protection Agency (NFPA) 99, Health Care Facilities.
Hyperbaric Modular Systems Inc.
HMS-5000-12
In Commercial Distribution
- 00860006478902 ()
- Hyperbaric chamber, stationary
cmAngio is intended to process screening mammograms to aid a qualified interpreting physician in the current manual process of identifying Breast Arterial Calcification (BAC).
cmAngio, a proprietary artificial intelligence (AI) based software, is intended to detect, at the study and breast level, the presence or absence of Breast Arterial Calcifications (BAC), an incidental finding in both Full Field Digital Mammogram (FFDM) and Digital Breast Tomosynthesis (DBT) screening mammograms. The device also marks BAC segments on thumbnails of images for localization of BAC.
The software is intended to be used by qualified interpreting physicians in parallel with breast screening mammography workflow. The device is not intended for primary interpretation of digital mammography images as used for breast cancer detection. The device results should not be used alone to make any diagnosis and/or treatment decisions.
Curemetrix, Inc.
V1.6
In Commercial Distribution
- 00860006442699 ()
- Radiology DICOM image processing application software
cmAngio is intended to process screening mammograms to aid a qualified interpreting physician in the current manual process of identifying Breast Arterial Calcification (BAC).
cmAngio, a proprietary artificial intelligence (AI) based software, is intended to detect, at the study and breast level, the presence or absence of Breast Arterial Calcifications (BAC), an incidental finding in both Full Field Digital Mammogram (FFDM) and Digital Breast Tomosynthesis (DBT) screening mammograms. The device also marks BAC segments on thumbnails of images for localization of BAC.
The software is intended to be used by qualified interpreting physicians in parallel with breast screening mammography workflow. The device is not intended for primary interpretation of digital mammography images as used for breast cancer detection and should not be used alone to make any diagnosis and/or treatment decisions.
cmAngio is for prescription use only.
Curemetrix, Inc.
V1.0
In Commercial Distribution
- 00860006442682 ()
- Radiology DICOM image processing application software
cmTriage is a passive notification for prioritization-only, parallel-workflow software tool used by radiologists to prioritize specific patients within the standard-of-care image worklist for 2D FFDM screening mammograms. cmTriage uses an artificial intelligence algorithm to analyze 2D FFDM screening mammograms and flags those that are suggestive of the presence of at least one suspicious finding at the exam level. These flags are viewed by the radiologist via their Picture Archiving and Communication System (PACS) worklist. The decision to use cmTriage codes and how to use cmTriage codes is ultimately up to the radiologist. cmTriage does not send a proactive alert directly to the radiologist.
Radiologists are responsible for reviewing each exam on a diagnostic viewer according to the current standard of care.
cmTriage is limited to the categorization of exams, does not provide any diagnostic information beyond triage and prioritization, does not remove images from the radiologist’s worklist, and should not be used in lieu of full patient evaluation, or relied upon to make or confirm diagnosis.
cmTriage is for prescription use only.
Curemetrix, Inc.
V1.0
In Commercial Distribution
- 00860006442668 ()
- Radiology DICOM image processing application software
Device Description
The sterile disposable, single-use surgical filter consists of a cylindrical container and dual filtrating system. Connection to the suction unit through the tubing is required to operate the device. The Bone Dust Trap is a filtration device for collecting bone dust and particles for subsequent bone graft implantation during various surgical procedures. The device can be emptied and further reused during a single operating procedure on the same patient.
Rim Medical Technologies Incorporated
1
In Commercial Distribution
- 00860006413903 ()
- Bone graft harvesting filter
PH Band
Medical Ingenuities, LLC
41111-01
In Commercial Distribution
- 00860006401702 ()
- 10860006401709 ()
PHB-001U
- Radial artery compression device
No Description
Analog Devices, Inc.
ADCP1100-AT-001
In Commercial Distribution
- 00860006382346 ()
- Wearable multiple vital physiological parameter monitoring system
No Description
Analog Devices, Inc.
ADCP-1100-BS-001
In Commercial Distribution
- 00860006382339 ()
- Wearable multiple vital physiological parameter monitoring system
No Description
Analog Devices, Inc.
ADCP1100-WB-001
In Commercial Distribution
- 00860006382322 ()
- Wearable multiple vital physiological parameter monitoring system
No Description
Analog Devices, Inc.
ADCP1100-PL-001
In Commercial Distribution
- 00860006382315 ()
- Wearable multiple vital physiological parameter monitoring system
No Description
Analog Devices, Inc.
ADI-CS-200-001
In Commercial Distribution
- 00860006382308 ()
- Wearable multiple vital physiological parameter monitoring system
Universal Knee Brace
HOME AIDE DIAGNOSTICS, INC.
UKBrace
In Commercial Distribution
- 10860006377899 ()
- 00860006377892 ()
- Tubular support bandage, non-latex, reusable
One handed use
No lancing device required
Automatic needle retraction
Lock out after use prevents needle stick injuries as well as cross-contamination
HOME AIDE DIAGNOSTICS, INC.
TrueCSafety50
In Commercial Distribution
- 10860006377851 ()
- 00860006377854 ()
- Needle Gauge: 30 Gauge
- Manual blood lancing device, single-use
One handed use
No lancing device required
Automatic needle retraction
Lock out after use prevents needle stick injuries as well as cross-contamination
HOME AIDE DIAGNOSTICS, INC.
TrueCSafety100
In Commercial Distribution
- 10860006377844 ()
- 00860006377847 ()
- Needle Gauge: 30 Gauge
- Manual blood lancing device, single-use
One handed use
No lancing device required
Automatic needle retraction
Lock out after use prevents needle stick injuries as well as cross-contamination
HOME AIDE DIAGNOSTICS, INC.
PureCSafety50
In Commercial Distribution
- 10860006377813 ()
- 00860006377816 ()
- Needle Gauge: 30 Gauge
- Manual blood lancing device, single-use
Nelson Water System's Water Purification System for Hemodialysis is intended to be used for purifying the water used in hemodialysis treatment. It removes organic, inorganic, and microbial contaminants from the water.
Nelson Environmental Technologies Inc
Complete System
In Commercial Distribution
- 00860006352127 ()
- Combination water purification system
The Nelson Sentinel Series Basic Chlorine Sentinel is a complete system that attaches to the drain of a hemodialysis water treatment system sample port. The Basic Chlorine Sentinel detects dissolved chlorine by an auxiliary meter detection technology, self-monitors for maintenance-required conditions, loss of electrical power, as well as two other system conditions such as flooding and the status of RO shutdown alarm. The device chlorine monitoring probe is preferably placed after the second carbon filter, before the RO machine or at the beginning of the patient water treatment loop.
The device has three components – a lockable master control enclosure, a lockable probe/tester enclosure, and the remote module installed in the patient area.
A chlorine concentration equal to or above the set-point (default: 0.10mg/L) will activate the buzzers and the red CHLORINE alarm indicators for as long as the condition exists. The buzzers can only be muted for 3 minutes (then automatically reset) for as long as the condition exists. The yellow AUTO-TEST OK/CL DETECTED indication will latch. The AUTO-TEST/CL DETECTED indication can be deactivated after the event by pressing the blue RESET PUSHBUTTON on the front cover of the controller.
A probe failure or the activation of one of the auxiliary input relays will activate the yellow MAINTENANCE needed indicators as well as the Buzzers which will remain activated as long as the condition exists. However, the buzzers can be muted by the key mute switch while the maintenance issue is being resolved.
Nelson Environmental Technologies Inc
NSS-BCS-001
In Commercial Distribution
- 00860006352103 ()
- Haemodialysis system chlorine monitor
Catalyst Live is a telepresence solution that enables collaboration in imaging, surgical, remote, and hybrid environments.
Ascend Cardiovascular LLC
7.2
In Commercial Distribution
- 00860006348007 ()
- Video consultation telemedicine system
Lumin serves as both a general-purpose sanitizing device for personal care items (e.g. cell phone, eyeglasses, keys, etc.) as well as CPAP accessories (e.g. hose, mask, and water chamber. In terms of CPAP sanitizer, there is no requirement for sterility or disinfection for single-patient re-use of CPAP accessories in the home. Most manufacturer instructions require simple cleaning with soap and water. Lumin is intended to be used as an adjunct to following the manufacturer’s instructions for routine cleaning but provides the convenience of bioburden reduction in 5 minutes. Lumin is designed to be used only with the CPAP accessories (i.e. CPAP Mask, hose, and water chamber), and not on the CPAP machine itself.
3B MEDICAL, INC.
LM3000
In Commercial Distribution
- 00860006339906 ()
- Ultraviolet device disinfection chamber
proudP is a mobile application intended for measuring voided volume of urine and urine flow rate using the sound recorded by microphone in mobile devices. This device can be used for assessment of voiding function. This device can be used at office and required to be used in a quiet environment. This device targets patients over 18 years of age.
Soundable Health, Inc.
SU-UFM-001
In Commercial Distribution
- 00860006184926 ()
- Home uroflowmetry software