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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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Silicone Gel Breast Implant, Smooth Round, Moderate High Profile, 115 cc
Sientra, Inc.
10521-115HP
Not in Commercial Distribution

  • 00812790020287 ()

  • Volume: 115 cc
10521-115HP

  • Silicone gel-filled breast implant, smooth-surface
Silicone Gel Breast Implant, Smooth Round, Moderate High Profile, 95 cc
Sientra, Inc.
10521-095HP
Not in Commercial Distribution

  • 00812790020270 ()

  • Volume: 95 cc
10521-095HP

  • Silicone gel-filled breast implant, smooth-surface
DBM 006010 PROGENIX PLUS PUTTY 10CC
MEDTRONIC SOFAMOR DANEK, INC.
006010
In Commercial Distribution

  • 00763000140571 ()

  • 10 CC volume


  • Bone matrix implant, human-derived
DBM 006005 PROGENIX PLUS PUTTY 5CC
MEDTRONIC SOFAMOR DANEK, INC.
006005
In Commercial Distribution

  • 00763000140564 ()

  • 5 CC volume


  • Bone matrix implant, human-derived
DBM 006002 PROGENIX PLUS PUTTY 2.5CC
MEDTRONIC SOFAMOR DANEK, INC.
006002
In Commercial Distribution

  • 00763000140557 ()

  • 2.5 CC volume


  • Bone matrix implant, human-derived
DBM 006001 PROGENIX PLUS PUTTY 1CC
MEDTRONIC SOFAMOR DANEK, INC.
006001
In Commercial Distribution

  • 00763000140540 ()

  • 1 CC volume


  • Bone matrix implant, human-derived
DBM 005110 PROGENIX PUTTY 10CC
MEDTRONIC SOFAMOR DANEK, INC.
005110
In Commercial Distribution

  • 00763000140533 ()

  • 10 CC volume


  • Bone matrix implant, human-derived
DBM 005005 PROGENIX PUTTY 5CC
MEDTRONIC SOFAMOR DANEK, INC.
005005
In Commercial Distribution

  • 00763000140526 ()

  • 5 CC volume


  • Bone matrix implant, human-derived
DBM 005001 PROGENIX PUTTY 1CC
MEDTRONIC SOFAMOR DANEK, INC.
005001
In Commercial Distribution

  • 00763000140519 ()

  • 1 CC volume


  • Bone matrix implant, human-derived
DBM 000505 PROGENIX PUTTY .5CC
MEDTRONIC SOFAMOR DANEK, INC.
000505
In Commercial Distribution

  • 00763000140502 ()

  • 0.5 CC volume


  • Bone matrix implant, human-derived
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