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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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Progreat Lambda - 04987350741028

Micro Catheter System
TERUMO CLINICAL SUPPLY CO., LTD.
CC*M1916DN
In Commercial Distribution

  • 54987350741023 ()
  • 04987350741028 ()

  • Length: 165 Centimeter
  • Catheter Inner Diameter: 0.48 Millimeter
  • Outer Diameter: 0.64 Millimeter
CCM1916DN

  • Vascular microcatheter

Progreat Lambda - 04987350741004

Micro Catheter System
TERUMO CLINICAL SUPPLY CO., LTD.
CC*M1916AN
In Commercial Distribution

  • 54987350741009 ()
  • 04987350741004 ()

  • Length: 165 Centimeter
  • Catheter Inner Diameter: 0.48 Millimeter
  • Outer Diameter: 0.64 Millimeter
CCM1916AN

  • Vascular microcatheter

Progreat Lambda - 04987350740984

Micro Catheter System
TERUMO CLINICAL SUPPLY CO., LTD.
CC*M1916SN
In Commercial Distribution

  • 04987350740984 ()
  • 54987350740989 ()

  • Length: 165 Centimeter
  • Catheter Inner Diameter: 0.48 Millimeter
  • Outer Diameter: 0.64 Millimeter
CCM1916SN

  • Vascular microcatheter

Corplex P - 00860471002572

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 - 00860471002565

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 - 00860471002558

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

Fortera - 00868201000188

Calcium compound bone void filler (10 cc)
Vivorte, Inc
10 cc
In Commercial Distribution

  • 00868201000188 ()


  • Bone matrix implant, synthetic, non-antimicrobial

Fortera - 00868201000171

Calcium compound bone void filler (5 cc)
Vivorte, Inc
5 cc
In Commercial Distribution

  • 00868201000171 ()
131133-05-S

  • Bone matrix implant, synthetic, non-antimicrobial

Fortera - 00868201000164

Calcium compound bone void filler (3 cc)
Vivorte, Inc
3 cc
In Commercial Distribution

  • 00868201000164 ()
131133-03-S

  • Bone matrix implant, synthetic, non-antimicrobial

Wizard CaP - 00868201000157

Calcium compound bone void filler (10 cc)
Vivorte, Inc
10 cc
Not in Commercial Distribution

  • 00868201000157 ()


  • Bone matrix implant, synthetic, non-antimicrobial

Wizard CaP - 00868201000140

Calcium compound bone void filler (5 cc)
Vivorte, Inc
5 cc
Not in Commercial Distribution

  • 00868201000140 ()


  • Bone matrix implant, synthetic, non-antimicrobial

Wizard CaP - 00868201000133

Calcium Bone Void Filler (3 cc)
Vivorte, Inc
3 cc
Not in Commercial Distribution

  • 00868201000133 ()


  • Bone matrix implant, synthetic, non-antimicrobial

Trabexus ® - 00868201000126

Calcium compound bone void filler (10 cc)
Vivorte, Inc
10 cc
Not in Commercial Distribution

  • 00868201000126 ()
131133-10

  • Bone matrix implant, synthetic, non-antimicrobial

Trabexus ® - 00868201000119

Calcium compound bone void filler (5 cc)
Vivorte, Inc
5 cc
Not in Commercial Distribution

  • 00868201000119 ()
131133-05

  • Bone matrix implant, synthetic, non-antimicrobial

Trabexus ® - 00868201000102

Calcium compound bone void filler (3cc)
Vivorte, Inc
3 cc
Not in Commercial Distribution

  • 00868201000102 ()
131133-03

  • Bone matrix implant, synthetic, non-antimicrobial

BELLAFILL - 00350224000141

Bellafill 1.5ml on 1.5cc syringe
SUNEVA MEDICAL, INC.
1.5 cc
In Commercial Distribution

  • 10350224000148 ()
  • 00350224000141 ()
  • 20350224000145 ()
  • 30350224000142 ()
GBF0115, GBF0215, GBF0315

  • Dermal tissue reconstructive material, animal-derived

BELLAFILL - 00350224000028

Bellafill 0.8ml on 1.0cc syringe
SUNEVA MEDICAL, INC.
1.0 cc
In Commercial Distribution

  • 00350224000028 ()
  • 10350224000025 ()
  • 20350224000022 ()
GBF0208, GBF0508

  • Dermal tissue reconstructive material, animal-derived

Trabexus® - W4146EB0010T0475

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

Trabexus® - W4146EB0005T0475

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

Trabexus® - W4146EB0003T0475

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
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