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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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Lateral Trial, 17mm, H12
SpineArt SA
JUL-IN 07 13-N
In Commercial Distribution

  • 07640178972667 ()
JUL-IN 07 13-N

  • Surgical implant/trial-implant/sizer holder, reusable
Lateral Trial, 17mm, H10
SpineArt SA
JUL-IN 07 12-N
In Commercial Distribution

  • 07640178972650 ()
JUL-IN 07 12-N

  • Surgical implant/trial-implant/sizer holder, reusable
Lateral Trial, 17mm, H08
SpineArt SA
JUL-IN 07 11-N
In Commercial Distribution

  • 07640178972643 ()
JUL-IN 07 11-N

  • Surgical implant/trial-implant/sizer holder, reusable
Lateral Trial, 17mm, H06
SpineArt SA
JUL-IN 07 10-N
In Commercial Distribution

  • 07640178972636 ()
JUL-IN 07 10-N

  • Surgical implant/trial-implant/sizer holder, reusable
VARIABLE ENDTIP ROD HOLDER
SpineArt SA
SPE-IN 00 38-N
In Commercial Distribution

  • 07640178972575 ()
SPE-IN 00 38-N

  • Surgical implant/trial-implant/sizer holder, reusable
SCREW HEAD ORIENTATOR BAYONETED
SpineArt SA
SPE-IN 00 06-N
In Commercial Distribution

  • 07640178972100 ()
SPE-IN 00 06-N

  • Surgical implant/trial-implant/sizer holder, reusable
ADJUSTABLE STOP NUT
SpineArt SA
SPE-IN 00 03-N
In Commercial Distribution

  • 07640178971189 ()
SPE-IN 00 03-N

  • Surgical implant/trial-implant/sizer holder, reusable
ADJUSTABLE STOP NUT
SpineArt SA
SPE-IN 00 02-N
In Commercial Distribution

  • 07640178971172 ()
SPE-IN 00 02-N

  • Surgical implant/trial-implant/sizer holder, reusable
No Description
Zimmer GmbH
01.04441.002
In Commercial Distribution

  • 00889024226760 ()
01.04441.002

  • Bone-resection orthopaedic reamer, reusable
GRAFT FUNNEL TUBE 5MM ID
SpineArt SA
SPE-US 00 12-N
In Commercial Distribution

  • 07640178985711 ()
SPE-US 00 12-N

  • Surgical implant/trial-implant/sizer holder, reusable
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