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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Device Name: CERASORB® Ortho Foam Mofidication: Mouldable Foam Indication for Use: Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x50x4 mm
In Commercial Distribution

  • ECURCOM2550 ()
1 x 5.0 cc

  • Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam Mofidication: Mouldable Foam Indication for Use: Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x25x2 mm
In Commercial Distribution

  • ECURCOM2525 ()
1 x 2.5 cc

  • Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam Mofidication: Mouldable Foam Indication for Use: Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x12x4 mm
In Commercial Distribution

  • ECURCOM2512 ()
1 x 1.2 cc

  • Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam Mofidication: Flexible Foam Stripe Indication for Use: Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
65x65x6 mm
In Commercial Distribution

  • ECURCOF6565 ()
1 x 25.0 cc

  • Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam Mofidication: Flexible Foam Stripe Indication for Use: Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x50x4 mm
In Commercial Distribution

  • ECURCOF2550 ()
1 x 0.5 cc

  • Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam Mofidication: Flexible Foam Stripe Indication for Use: Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x100x4 mm
In Commercial Distribution

  • ECURCOF25100 ()
1 x 10.0 cc

  • Bone matrix implant, composite
Device Name: Matriform Strip Indication for Use: Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process
curasan AG
100x25x4mm
In Commercial Distribution

  • ECUR449100 ()
1 x 10 cc

  • Bone matrix implant, composite
Device Name: Matriform SI-Strip Indication for Use: Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process
curasan AG
50x25x4 mm
In Commercial Distribution

  • ECUR449050 ()
1 x 5 cc

  • Bone matrix implant, composite
Device Name: Matriform Strip Mofidication: Flexible Foam Indication for Use: Matriform Strip is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Strip resorbs and is replaced with bone during healing process.
curasan AG
25x100x4mm
In Commercial Distribution

  • ECUR429100 ()
1 x 10 cc

  • Bone matrix implant, composite
Device Name: Matriform Strip Mofidication: Flexible Foam Indication for Use: Matriform Strip is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Strip resorbs and is replaced with bone during healing process.
curasan AG
25x50x4 mm
In Commercial Distribution

  • ECUR429050 ()
1 x 5 cc

  • Bone matrix implant, composite
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