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MICRO ARTERY CLAMP SINGLE
TYPE 5, 2.0 - 5.0 MM
LENGTH 36 MM
Gimmi GmbH
CC.1158.20
In Commercial Distribution
- 04049047694809 ()
CC.1158.20
- Surgical A/V-shaped microvessel clamp
MICRO ARTERY CLAMP SINGLE
TYPE 4, 1.5 - 3.3 MM
LENGTH 24 MM
Gimmi GmbH
CC.1158.15
In Commercial Distribution
- 04049047694793 ()
CC.1158.15
- Surgical A/V-shaped microvessel clamp
MICRO ARTERY CLAMP DOUBLE
ADJUSTABLE, TYPE 2, 0.6 - 1.4 MM
LENGTH 11 MM
Gimmi GmbH
CC.1160.06
In Commercial Distribution
- 04049047694878 ()
CC.1160.06
- Surgical A/V-shaped microvessel clamp
MICRO ARTERY CLAMP SINGLE
TYPE 2, 0.6 - 1.4 MM
LENGTH 11 MM
Gimmi GmbH
CC.1158.06
In Commercial Distribution
- 04049047694779 ()
CC.1158.06
- Surgical A/V-shaped microvessel clamp
No Description
TEKNIMED
11 CC
Not in Commercial Distribution
- 03760177046344 ()
183901000
- Vertebral bone filler, non-bioabsorbable
No Description
TEKNIMED
11 CC
Not in Commercial Distribution
- 03760177043947 ()
183901000
- Vertebral bone filler, non-bioabsorbable
CommunicationConsole is part of NordicNeuroLab’s Audio System.
The AudioSystem allows auditory signals from the stimulus presentation PC to enter the scanner room and to be presented to the patient wearing a set of headphones. The Communication Console allows the operator to adjust the sounds from the PC and to speak directly to the patient through a built-in microphone.
Nordicneurolab AS
CC 2.3
In Commercial Distribution
- 07090042053044 ()
- Auditory stimulator
OSSIX™ BONE is a biodegradable, osteoconductive, and biocompatible bone grafting
material intended for guided tissue and bone regeneration. The OSSIX™ BONE matrix is
composed of 80% synthetic crystalline non-sintered hydroxylapatite and 20% collagen,
which is derived from veterinary certified pigs and is purified and cross-linked.
DATUM DENTAL LTD
0.250 cc
In Commercial Distribution
- 07290015477222 ()
- Height: 5 Millimeter
- Length: 10 Millimeter
- Depth: 5 Millimeter
- 0.250 cc
OXB0250
- Dental bone matrix implant, synthetic
OSSIX™ BONE is a biodegradable, osteoconductive, and biocompatible bone grafting
material intended for guided tissue and bone regeneration. The OSSIX™ BONE matrix is
composed of 80% synthetic crystalline non-sintered hydroxylapatite and 20% collagen,
which is derived from veterinary certified pigs and is purified and cross-linked.
DATUM DENTAL LTD
0.125 cc
In Commercial Distribution
- 07290015477215 ()
- 0.125 cc
- Depth: 5 Millimeter
- Length: 5 Millimeter
- Height: 5 Millimeter
OXB0125
- Dental bone matrix implant, synthetic
OssDsign Catalyst is an osteoconductive, resorbable, porous, 100% nanosynthetic calcium phosphate bone void filler. OssDsign Catalyst contains 5.8 wt% silicon-substituted calcium phosphate granules suspended in a resorbable polymer gel. The final, finished OssDsign Catalyst is 30 wt% granules and 70 wt% polymer gel. The high surface area porous granules have been designed to deliver consistent and rapid bone ingrowth, remodeling and cell-mediated resorption during the bone healing process. The aqueous polymer gel phase binds the highly porous granules into a moldable, pliable formulation which enables OssDsign Catalyst to be implanted directly from the packaging without any further gelation, mixing or graft setting time. OssDsign Catalyst is provided sterile to the end user in 2.5 cc, 5 cc and 10 cc sizes. (510(k) no. K193075)
Ossdsign AB
1 cc
In Commercial Distribution
- 07350086550733 ()
104010
- Bone matrix implant, synthetic, non-antimicrobial
Calcium compound bone void filler with DBM (10 cc), previously sold under Trabexus® EB brand name.
Vivorte, Inc
10 cc
In Commercial Distribution
- W4146EB0010T0475 ()
130703-10
- Cadaveric-donor/synthetic mineral bone graft
Calcium compound bone void filler with DBM (5cc), Previously sold under Trabexus® EB brand name.
Vivorte, Inc
5 cc
In Commercial Distribution
- W4146EB0005T0475 ()
130703-05
- Cadaveric-donor/synthetic mineral bone graft
Calcium compound bone void filler with DBM (3 cc), previously sold under Trabexus® EB brand name.
Vivorte, Inc
3 cc
In Commercial Distribution
- W4146EB0003T0475 ()
130703-03
- Cadaveric-donor/synthetic mineral bone graft
No Description
PARKS MEDICAL ELECTRONICS, INC.
812-1-901 CC
In Commercial Distribution
- 00816787020427 ()
- Laser Doppler blood flowmeter
No Description
PARKS MEDICAL ELECTRONICS, INC.
812-1-800 CC
In Commercial Distribution
- 00816787020410 ()
- Laser Doppler blood flowmeter
OSSIX™ BONE is a biodegradable, osteoconductive, and biocompatible bone grafting
material intended for guided tissue and bone regeneration. The OSSIX™ BONE matrix is
composed of 80% synthetic crystalline non-sintered hydroxylapatite and 20% collagen,
which is derived from veterinary certified pigs and is purified and cross-linked.
DATUM DENTAL LTD
0.500 cc
In Commercial Distribution
- 07290015477253 ()
- Height: 5 Millimeter
- Length: 10 Millimeter
- Depth: 10 Millimeter
- 0.500 cc
OXB0500
- Dental bone matrix implant, synthetic
Corplex P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Corplex P/Theracor P/Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
4 cc
In Commercial Distribution
- 00860471002572 ()
CP-0040
- Animal-derived wound matrix dressing
Corplex P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Corplex P/Theracor P/Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
2 cc
In Commercial Distribution
- 00860471002565 ()
CP0020
- Animal-derived wound matrix dressing
Corplex P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Corplex P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
1 cc
In Commercial Distribution
- 00860471002558 ()
CP-0010
- Animal-derived wound matrix dressing
Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
4 cc
In Commercial Distribution
- 00850039927362 ()
AP-0040
- Animal-derived wound matrix dressing
Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
2 cc
In Commercial Distribution
- 00850039927355 ()
AP-0020
- Animal-derived wound matrix dressing
Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
1 cc
In Commercial Distribution
- 00850039927348 ()
AP-0010
- Animal-derived wound matrix dressing
Device Name: Curasan OSSEOLIVE® DENTAL
lndications for Use:
OSSEOLIVE® DENTAL is indicated for applications in oral and
maxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled
(artificial or degenerative) bone defects, e.g.:
- Defects after the extirpation of bone cysts
- Augmentation of an atrophied alveolar ridge
- Sinus lift or sinus floor elevation (subantral augmentation)
- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge
- Filling of extraction defects to create an implant bed
- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects
- Defects after operative removal of retained teeth or corrective osteotomies
curasan AG
250-1000µm
In Commercial Distribution
- ECURL20M0250 ()
- ECURL20M02505 ()
5x2.0 cc
- Dental bone matrix implant, synthetic
CC527 Multi-Level Carton
Rna Medical Division
CC527 Multi-Level
In Commercial Distribution
- 10851290002444 ()
CC 527
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, control
CC527 Level 3 carton
Rna Medical Division
CC527 Level 3
In Commercial Distribution
- 10851290002437 ()
CC 527-3
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, control
CC527 Level 2 Carton
Rna Medical Division
CC527 Level 2
In Commercial Distribution
- 10851290002420 ()
CC 527-2
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, control
CC527 Level 1 Carton
Rna Medical Division
CC527 Level 1
In Commercial Distribution
- 10851290002413 ()
CC 527-1
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, control
Diatro•Hypoclean CC hypochlorite cleaning concentrate is a stabilized and micro-filtered concentrated hypochlorite solution for intensive oxidative cleaning, rinsing and washing of hematology analyzers’ capillaries, tubing and chambers, removing blood component precipitates and lipoprotein deposits on all hematology analyzers.
Diatron Medicinai Instrumentumok Laboratoriumi Diagnosztikai Fejleszto-Gyarto Zartkoruen Mukodo Reszvenytarsasag
D801
In Commercial Distribution
- 15999883586638 ()
- 05999883586631 ()
- Total Volume: 100 Milliliter
D8011
- Wash/cleaning solution IVD, automated/semi-automated system
Synthetic bone void filler for orthopedic applications
NOVABONE PRODUCTS, LLC
NB2508SX
In Commercial Distribution
- 00813909013206 ()
- 8.0cc
NB2508SX
- Bone matrix implant, synthetic, non-antimicrobial
No Description
I3 IMPLANT LLC
i3CCAA
In Commercial Distribution
- 00850008541803 ()
- Dental implant suprastructure, temporary, preformed, reusable
No Description
I3 IMPLANT LLC
i3CCSA
In Commercial Distribution
- 00850008541797 ()
- Dental implant suprastructure, temporary, preformed, reusable
OsteoBoost is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, OsteoBoost resorbs and is later replaced by natural bone. It provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.
OsteoBoost is an osteoconductive putty that is intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium.
The putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs.
BERKELEY ADVANCED BIOMATERIALS, LLC
OB-10P
In Commercial Distribution
- 00816125023400 ()
OB-10P
- Bone matrix implant, synthetic, non-antimicrobial
OsteoBoost is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, OsteoBoost resorbs and is later replaced by natural bone. It provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.
OsteoBoost is an osteoconductive putty that is intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium.
The putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs.
BERKELEY ADVANCED BIOMATERIALS, LLC
OB-05P
In Commercial Distribution
- 00816125023394 ()
OB-05P
- Bone matrix implant, synthetic, non-antimicrobial
Compactor
SpineArt SA
TRY-IN 01 00-N
In Commercial Distribution
- 07640151081881 ()
TRY-IN 01 00-N
- Bone graft packing block
Convex Trial D14 H12
SpineArt SA
TRY-IA 14 12-N
In Commercial Distribution
- 07640151081836 ()
TRY-IA 14 12-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H11
SpineArt SA
TRY-IA 14 11-N
In Commercial Distribution
- 07640151081829 ()
TRY-IA 14 11-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H10
SpineArt SA
TRY-IA 14 10-N
In Commercial Distribution
- 07640151081812 ()
TRY-IA 14 10-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H09
SpineArt SA
TRY-IA 14 09-N
In Commercial Distribution
- 07640151081805 ()
TRY-IA 14 09-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H08
SpineArt SA
TRY-IA 14 08-N
In Commercial Distribution
- 07640151081799 ()
TRY-IA 14 08-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H07
SpineArt SA
TRY-IA 14 07-N
In Commercial Distribution
- 07640151081782 ()
TRY-IA 14 07-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H06
SpineArt SA
TRY-IA 14 06-N
In Commercial Distribution
- 07640151081775 ()
TRY-IA 14 06-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D14 H05
SpineArt SA
TRY-IA 14 05-N
In Commercial Distribution
- 07640151081768 ()
TRY-IA 14 05-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H12
SpineArt SA
TRY-IA 12 12-N
In Commercial Distribution
- 07640151081751 ()
TRY-IA 12 12-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H11
SpineArt SA
TRY-IA 12 11-N
In Commercial Distribution
- 07640151081744 ()
TRY-IA 12 11-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H10
SpineArt SA
TRY-IA 12 10-N
In Commercial Distribution
- 07640151081737 ()
TRY-IA 12 10-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H09
SpineArt SA
TRY-IA 12 09-N
In Commercial Distribution
- 07640151081720 ()
TRY-IA 12 09-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H08
SpineArt SA
TRY-IA 12 08-N
In Commercial Distribution
- 07640151081713 ()
TRY-IA 12 08-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H07
SpineArt SA
TRY-IA 12 07-N
In Commercial Distribution
- 07640151081706 ()
TRY-IA 12 07-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H06
SpineArt SA
TRY-IA 12 06-N
In Commercial Distribution
- 07640151081690 ()
TRY-IA 12 06-N
- Surgical implant/trial-implant/sizer holder, reusable
Convex Trial D12 H05
SpineArt SA
TRY-IA 12 05-N
In Commercial Distribution
- 07640151081683 ()
TRY-IA 12 05-N
- Surgical implant/trial-implant/sizer holder, reusable