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The Device is intended for orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed. The devices are intended to be single used only.
Forestadent Bernhard Förster GmbH
C713-1613
In Commercial Distribution
- EFORC7131613 ()
- Height: .018 Inch
C713-1613
- Orthodontic bracket, ceramic
The Device is intended for orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed. The devices are intended to be single used only.
Forestadent Bernhard Förster GmbH
C713-1611
In Commercial Distribution
- EFORC7131611 ()
- Height: .022 Inch
C713-1611
- Orthodontic bracket, ceramic
The Device is intended for orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed. The devices are intended to be single used only.
Forestadent Bernhard Förster GmbH
C713-1513
In Commercial Distribution
- EFORC7131513 ()
- Height: .018 Inch
C713-1513
- Orthodontic bracket, ceramic
The Registration Pointer EM-D is an electromagnetically tracked instrument with a rounded, blunt tip that is used to register the patient anatomy. The location of the instrument is referenced relative to a patient tracker affixed to the patient’s anatomy. The pointer connects to the Hybrid Navigation Unit EM via an integrated cable.
The Precision Pointer EM-D is provided non-sterile and is intended intended for high-level disinfection only. It is intended to be used prior to surgical draping while the patient environment is not covered under sterile drape. The Registration Pointer EM-D is reusable.
Scopis GmbH
1.0
In Commercial Distribution
- B057U1029030 ()
U1 029 03
- Electromagnetic surgical navigation device tracking system
The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.
Ascension Orthopedics, Inc.
MGT89040PPH
In Commercial Distribution
- 10381780116479 ()
- M268MGT89040PPH1 ()
- .771 in L x .549 in W x .472 in H; Size 40
MGT89040PPH
- Partial metatarsophalangeal joint prosthesis
The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.
Ascension Orthopedics, Inc.
MGT89030PPH
In Commercial Distribution
- 10381780116455 ()
- M268MGT89030PPH1 ()
- .721 in L x .520 in W x .433 in H; Size 30
MGT89030PPH
- Partial metatarsophalangeal joint prosthesis
The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.
Ascension Orthopedics, Inc.
MGT89020PPH
In Commercial Distribution
- 10381780116431 ()
- M268MGT89020PPH1 ()
- .660 in L x .492 in W x .394 in H; Size 20
MGT89020PPH
- Partial metatarsophalangeal joint prosthesis
The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.
Ascension Orthopedics, Inc.
MGT89010PPH
In Commercial Distribution
- 10381780116417 ()
- M268MGT89010PPH1 ()
- .606 in L x .463 in W x .354 in H; Size 10
MGT89010PPH
- Partial metatarsophalangeal joint prosthesis
The 1.2mL Skyrizi On-Body Injector is designed to be used in conjunction with a pre-filled cartridge assembly containing a 180mg/1.2mL dose of risankizumab-rzaa drug product. The single use device is designed for subcutaneous injection. The device is pre-sterilized and pre-programmed. The device is co-packaged with the drug product and is not marketed separately.
ABBVIE INC.
19558594
In Commercial Distribution
- 48054083023968 ()
- Width: 41 Millimeter
- Length: 85 Millimeter
- Height: 22.5 Millimeter
19558594
- Subcutaneous self-injection aid
The 2.4mL Skyrizi On-Body Injector is designed to be used in conjunction with a pre-filled cartridge assembly containing a 360mg/2.4mL dose of risankizumab-rzaa drug product. The single use device is designed for subcutaneous injection. The device is pre-sterilized and pre-programmed. The device is co-packaged with the drug product and is not marketed separately.
ABBVIE INC.
19558595
In Commercial Distribution
- 48054083023234 ()
- Width: 41 Millimeter
- Length: 85 Millimeter
- Height: 22.5 Millimeter
- Subcutaneous self-injection aid