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TAPE LST LEVEL DETECTOR MOUNT
MEDTRONIC, INC.
LST
In Commercial Distribution
- 00613994258106 ()
- Cardiopulmonary bypass system centrifugal pump drive unit
DETECTOR BD14 BUBBLE PEDIATRIC
MEDTRONIC, INC.
BD14
In Commercial Distribution
- 00613994258090 ()
- Cardiopulmonary bypass system air bubble/fluid level detector
SYSTEM ACS500 AUTOCLAMP
MEDTRONIC, INC.
ACS500
In Commercial Distribution
- 00613994258250 ()
- Medical tubing clip/clamp, temporary, non-calibrated, reusable
SENSOR LS100 LEVEL DETECTOR LOW PROF 12L
MEDTRONIC, INC.
LS100
In Commercial Distribution
- 00613994757616 ()
- Cardiopulmonary bypass system centrifugal pump drive unit
The Hand of Hope (HOH) is a therapy device (exoskeleton) used for neuromuscular rehabilitation
of the hand and forearm. HOH functions as a biofeedback device where surface electromyography
(sEMG) electrodes depict voluntary muscle activation. The depicted signals are processed and
simplified, and can be seen by a convenient presentation of visual feedback. The sEMG readout
enables patients to monitor the fundamental neuromuscular functional state. Therefore, impairment,
functional limitation and impaired volitional movement due to stroke or other neurologic or
orthopaedic diseases can be easily presented and utilized by a sensory signal. Patient’s attention is
drawn to the task through a visually displayed sEMG signal and consequently used for the initiation
of the motor task. This biofeedback mechanism promotes motor learning via interactive use. In
particular, stroke is one of the leading causes of adult disability, and hand rehabilitation after stroke
is a very challenging part thereof. However, it is well known that sensory signals such as visual
sensory inputs reach the motor cortex and modulate motor cortex function and excitability, and
therefore can improve motor learning. Since active participation and initiation of the movement is the
key to success, using the biofeedback system, HOH motivates patients to actively interact with the
system during an sEMG controlled task-related training regime
Rehab-Robotics Company Limited
HOH4-SM-LR-W
In Commercial Distribution
- 04897113220014 ()
- Virtual-display rehabilitation system, powered-support, upper-limb
SYSTEM ACS500 AUTOCLAMP KIT NON RoHS
MEDTRONIC, INC.
ACS500
In Commercial Distribution
- 00643169315747 ()
- Medical tubing clip/clamp, temporary, non-calibrated, reusable
FORESIGHT MEDIUM SENSOR
Edwards Lifesciences LLC
FSESM
In Commercial Distribution
- 50690103211332 ()
- 00690103211337 ()
- Medium
FSESM
- Tissue saturation oximeter sensor, single-use
FORESIGHT SMALL SENSOR
Edwards Lifesciences LLC
FSESS
In Commercial Distribution
- 50690103211325 ()
- 00690103211320 ()
- Small
FSESS
- Tissue saturation oximeter sensor, single-use
FORESIGHT NON-ADHESIVE SMALL SENSOR
Edwards Lifesciences LLC
FSESNS
In Commercial Distribution
- 50690103211318 ()
- 00690103211313 ()
- Small
FSESNS
- Tissue saturation oximeter sensor, single-use
SM Implant System is a root-form threaded dental implant made of Grade 3 and Grade 4 titanium. The implant is produced by machining process, followed by grit blasting and cleaning. It is available in diameters 3.8, 4.5 and 5.3mm, and lengths from 8mm to 14mm. It is placed via one or two stage surgery and the functional loading can be from immediated to delay.
DIO Corporation
AGT 50614
In Commercial Distribution
- 08806195928776 ()
- Ø5.5X4.1mm
AGT 50614
- Screw endosteal dental implant, two-piece
The DIO Implant System includes one-stage fixture and two-stage fixture made of titanium. These implants are surgically inserted into the upper and/or lower jawbone, and serve as a substitute or replacement tooth root providing a stable foundation for restorations.
DIO Corporation
AAI 35025NB
In Commercial Distribution
- 08806195926697 ()
- Ø3.5(25˚)mm
AAI 35025NB
- Screw endosteal dental implant, two-piece
The DIO Implant System includes one-stage fixture and two-stage fixture made of titanium. These implants are surgically inserted into the upper and/or lower jawbone, and serve as a substitute or replacement tooth root providing a stable foundation for restorations.
DIO Corporation
AAI 35025NA
In Commercial Distribution
- 08806195926680 ()
- Ø3.5(25˚)mm
AAI 35025NA
- Screw endosteal dental implant, two-piece
The DIO Implant System includes one-stage fixture and two-stage fixture made of titanium. These implants are surgically inserted into the upper and/or lower jawbone, and serve as a substitute or replacement tooth root providing a stable foundation for restorations.
DIO Corporation
AAI 35015NB
In Commercial Distribution
- 08806195926642 ()
- Ø3.5(15˚)mm
AAI 35015NB
- Screw endosteal dental implant, two-piece
The DIO Implant System includes one-stage fixture and two-stage fixture made of titanium. These implants are surgically inserted into the upper and/or lower jawbone, and serve as a substitute or replacement tooth root providing a stable foundation for restorations.
DIO Corporation
AAI 35015NA
In Commercial Distribution
- 08806195926635 ()
- Ø3.5(15˚)mm
AAI 35015NA
- Screw endosteal dental implant, two-piece
The DIO Biotite-H Implant System is comprised of dental implant, surgical instruments and prosthetic components. The DIG BIOTITE -H Implant System is designed for conventional two-stage procedures for single and multiple unit prosthetics. The DIO Biotite-H Implant System's screw-form dental implant consist of machined titanium. Screw's Diameter: Φ3.8mm, Φ4.1mm, Φ4.5mm, Φ4.8mm, Φ5.3mm. Length: 8.0mm, 10.mm, 12.0mm, 14.0mm. The implant's raw material is titanium and its alloys for surgical implant applications (as perASTM-F-67, A-STM-F-136). The special implant surface is consists of 100% calcium phosphate(CaHPO 42H20). BioTite-H Implant System is an electrochemically deposited calcium phosphate coating based upon abiomimetic process in which implants are coated in an electrolytic bath with a 15+±- 5μm thin bioactive layer of a calcium phosphate composite. Biotite -H Implant System composed of the two calciumphosphates brushite(>95% )and HA(<5%).
DIO Corporation
SFR 4508H
In Commercial Distribution
- 08806195922071 ()
- ® Ø4.5X8mm
SFR 4508H
- Screw endosteal dental implant, two-piece
The DIO Biotite-H Implant System is comprised of dental implant, surgical instruments and prosthetic components. The DIG BIOTITE -H Implant System is designed for conventional two-stage procedures for single and multiple unit prosthetics. The DIO Biotite-H Implant System's screw-form dental implant consist of machined titanium. Screw's Diameter: Φ3.8mm, Φ4.1mm, Φ4.5mm, Φ4.8mm, Φ5.3mm. Length: 8.0mm, 10.mm, 12.0mm, 14.0mm. The implant's raw material is titanium and its alloys for surgical implant applications (as perASTM-F-67, A-STM-F-136). The special implant surface is consists of 100% calcium phosphate(CaHPO 42H20). BioTite-H Implant System is an electrochemically deposited calcium phosphate coating based upon abiomimetic process in which implants are coated in an electrolytic bath with a 15+±- 5μm thin bioactive layer of a calcium phosphate composite. Biotite -H Implant System composed of the two calciumphosphates brushite(>95% )and HA(<5%).
DIO Corporation
SFN 4110H
In Commercial Distribution
- 08806195922040 ()
- ® Ø4.1X10mm
SFN 4110H
- Screw endosteal dental implant, two-piece
The DIO UF HSA Internal Sub-Merged Implant System is comprised of dental implants, Superstructures, Instruments for prosthetics and Surgical Instruments.
The DIO UF HSA Internal Sub-Merged Implant System is specially designed for using in dental implant surery. A successfully osseointegrated implant willl achieve a firm implant when the fixture is operated under controlled conditions, per well known clinical studies. There are intended for use in partially or fully edendulous mandibles and maxillae, in support of single or multiple-unit restorations.
The superstructures consist of screws(Cover Screw, Coping Screw), abutments(Screw retained type, Cemented retained type, Over denture retained type), Solid protect cap.
The screws are made of commercial pure titanium, grade 4(ASTM F67) and Ti-6A1-4VELI(ASTM F136) intended to be used in a narrow tooth gap after implant insertion. And the screw is used to protect exposed top of the implant or to attach the abutment to implant.
DIO Corporation
SSPI 4510H
In Commercial Distribution
- 08806195916704 ()
- Ø4.5X10.0mm Hex
SSPI 4510H
- Screw endosteal dental implant, two-piece
The DIO Steady External Implant System is comprised of dental implants, and superstructures.
The DIO Steady External Implant System is specially designed for use in dental implant surgery. A successfully osseointegrated implant will achieve a firm implant when surgically implanted under controlled conditions, per well known clinical studies. There are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations.
DIO Corporation
ESF 4515R
In Commercial Distribution
- 08806195920275 ()
- Ø4.5X15mm
ESF 4515R
- Screw endosteal dental implant, two-piece
LASER WORKING INSERT 30 color code black, round, without pivot angle limitation, distal sheath end slanted, compatible with sheaths 8632027, 8655345, and telescopes Ø 4mm, 0°-30°, bayonet-cap, reusable
Richard Wolf GmbH
8632912
In Commercial Distribution
- 04055207018248 ()
- Angle: 30 degree
8632.912
- Rigid endoscope working guide
LASER WORKING INSERT 12/30 color code green, round, with pivot angle limitation, distal sheath end slanted, compatible with sheaths 8632027, 8655345, and telescopes Ø 4mm, 0°-30°, bayonet-cap, reusable
Richard Wolf GmbH
8632911
In Commercial Distribution
- 04055207018231 ()
8632.911
- Rigid endoscope working guide
"Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a
temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage
revision procedure due to a septic process.
The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone
cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder
following removal of the existing humeral and glenoideal cavity implants and debridement.
SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.
The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy
(standard treatment approach to an infection).
The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is
not intended for use more than 180 days, at which time it must be explanted and permanent
devices implanted or another appropriate treatment performed (e.g. resection arthroplasty,
fusion, etc.).
Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low
viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated
for patients who will consistently follow activity limitation throughout the implant period.
The device can exclusively be used by competent healthcare personnel who has complete
scientific and anatomical knowledge."
G21 SRL
900001 144818
In Commercial Distribution
- 08058964726087 ()
- Orthopaedic cement spacer mould
Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a
temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage
revision procedure due to a septic process.
The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone
cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder
following removal of the existing humeral and glenoideal cavity implants and debridement.
SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.
The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy
(standard treatment approach to an infection).
The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is
not intended for use more than 180 days, at which time it must be explanted and permanent
devices implanted or another appropriate treatment performed (e.g. resection arthroplasty,
fusion, etc.).
Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low
viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated
for patients who will consistently follow activity limitation throughout the implant period.
The device can exclusively be used by competent healthcare personnel who has complete
scientific and anatomical knowledge.
G21 SRL
900001 124818
In Commercial Distribution
- 08058964726070 ()
- Orthopaedic cement spacer mould
Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a
temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage
revision procedure due to a septic process.
The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone
cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder
following removal of the existing humeral and glenoideal cavity implants and debridement.
SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.
The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy
(standard treatment approach to an infection).
The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is
not intended for use more than 180 days, at which time it must be explanted and permanent
devices implanted or another appropriate treatment performed (e.g. resection arthroplasty,
fusion, etc.).
Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low
viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated
for patients who will consistently follow activity limitation throughout the implant period.
The device can exclusively be used by competent healthcare personnel who has complete
scientific and anatomical knowledge.
G21 SRL
900001 124215
In Commercial Distribution
- 08058964726063 ()
- Orthopaedic cement spacer mould
Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a
temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage
revision procedure due to a septic process.
The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone
cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder
following removal of the existing humeral and glenoideal cavity implants and debridement.
SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.
The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy
(standard treatment approach to an infection).
The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is
not intended for use more than 180 days, at which time it must be explanted and permanent
devices implanted or another appropriate treatment performed (e.g. resection arthroplasty,
fusion, etc.).
Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low
viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated
for patients who will consistently follow activity limitation throughout the implant period.
The device can exclusively be used by competent healthcare personnel who has complete
scientific and anatomical knowledge.
G21 SRL
900001 104818
In Commercial Distribution
- 08058964726056 ()
- Orthopaedic cement spacer mould
Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a
temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage
revision procedure due to a septic process.
The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone
cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder
following removal of the existing humeral and glenoideal cavity implants and debridement.
SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.
The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy
(standard treatment approach to an infection).
The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is
not intended for use more than 180 days, at which time it must be explanted and permanent
devices implanted or another appropriate treatment performed (e.g. resection arthroplasty,
fusion, etc.).
Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low
viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated
for patients who will consistently follow activity limitation throughout the implant period.
The device can exclusively be used by competent healthcare personnel who has complete
scientific and anatomical knowledge.
G21 SRL
900001 104215
In Commercial Distribution
- 08058964726049 ()
- Orthopaedic cement spacer mould
Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold a
temporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stage
revision procedure due to a septic process.
The temporary prosthesis is molded using low viscosity polymethylmethacrylate bone
cement and inserted into the humeral medullary canal and glenoid cavity of the shoulder
following removal of the existing humeral and glenoideal cavity implants and debridement.
SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.
The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy
(standard treatment approach to an infection).
The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds is
not intended for use more than 180 days, at which time it must be explanted and permanent
devices implanted or another appropriate treatment performed (e.g. resection arthroplasty,
fusion, etc.).
Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (low
viscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicated
for patients who will consistently follow activity limitation throughout the implant period.
The device can exclusively be used by competent healthcare personnel who has complete
scientific and anatomical knowledge.
G21 SRL
900001 084215
In Commercial Distribution
- 08058964724977 ()
- Orthopaedic cement spacer mould
Cook-Swartz Doppler Flow Probe Long Cuff
Cook Vandergrift Inc.
G03014
In Commercial Distribution
- 00827002030145 ()
- 10827002030142 ()
DP-SDP002
- Blood flowmeter catheter, Doppler
Cook-Swartz Doppler Flow Probe Extension Cable
Cook Vandergrift Inc.
G21364
In Commercial Distribution
- 00827002213647 ()
- 10827002213644 ()
DP-CAB01
- Electrical-only medical device connection cable, single-use
Cook-Swartz Doppler Flow Probe Standard Cuff
Cook Vandergrift Inc.
G21363
In Commercial Distribution
- 00827002213630 ()
- 10827002213637 ()
DP-SDP001
- Blood flowmeter catheter, Doppler
Ultra Band-Lok® is intended for use as an orthodontic band cement and for occlusal buildups.
This product is blue shade.
RELIANCE ORTHODONTIC PRODUCTS INC
UBLBPP
In Commercial Distribution
- D798UBLBPP0 ()
UBLBPP
- Dental composite resin