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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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CMC, Metacarpal Trial Size 20
Stryker GmbH
17-0186
In Commercial Distribution

  • 00886385025650 ()

  • SIZE 20, Metacarpal


  • Surgical implant template, reusable
PreFlex MCP Sizer, Size 20
Stryker GmbH
MCPX-205
In Commercial Distribution

  • 00886385025346 ()
MCPX-205

  • Surgical implant template, reusable
MCP PreFlex Implant Size 20
Stryker GmbH
MCPX-20
In Commercial Distribution

  • 00886385025339 ()
MCPX-20

  • Metacarpophalangeal joint prosthesis, one-piece
Silicone PIP Implant Size 20
Stryker GmbH
PIP-20
In Commercial Distribution

  • 00886385021539 ()
PIP-20

  • Proximal interphalangeal joint prosthesis, one-piece
TL,BOLT, 12MM, QTY. 20
ORTHOFIX SRL
1
In Commercial Distribution

  • 18033509853524 ()

  • Width: 129 Millimeter
54-1050M

  • External orthopaedic fixation system, single-use
TL,BOLT, 16MM, QTY. 20
ORTHOFIX SRL
1
In Commercial Distribution

  • 18033509853500 ()

  • Width: 127 Millimeter
54-1010M

  • External orthopaedic fixation system, single-use
NUTS & WASHERS (PACK OF 20)
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860733 ()
81022

  • Implantable bone washer
WIRE COVERS (PACK OF 20)
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860597 ()
80200

  • External orthopaedic fixation system, reusable
SmokeStop - Smoke Evacuation 20" Tubing
Operating Room Innovations, Inc.
SS-EVAC20
Not in Commercial Distribution

  • 26975085708333 ()
  • 06975085708339 ()
SS-EVAC20

  • Surgical plume evacuation system tube
DRIVER 4360420 20/25MM EXPANSION
MEDTRONIC SOFAMOR DANEK, INC.
4360420
In Commercial Distribution

  • 00763000864781 ()


  • Surgical screwdriver, reusable
CURETTE EX1222010 20 DEG. PULL
MEDTRONIC SOFAMOR DANEK, INC.
EX1222010
In Commercial Distribution

  • 00763000829421 ()


  • Bone curette, reusable
BASE HL Trial, 14x42x36mm 20°
Nuvasive, Inc.
6959262
In Commercial Distribution

  • 00887517705044 ()


  • Spinal implant trial
BASE HL Trial, 12x42x36mm 20°
Nuvasive, Inc.
6959261
In Commercial Distribution

  • 00887517705037 ()


  • Spinal implant trial
BASE HL Trial, 10x42x36mm 20°
Nuvasive, Inc.
6959260
In Commercial Distribution

  • 00887517705020 ()


  • Spinal implant trial
BASE HL Trial, 6x42x36mm 20°
Nuvasive, Inc.
6959258
In Commercial Distribution

  • 00887517705006 ()


  • Spinal implant trial
BASE HL Trial, 4x42x36mm 20°
Nuvasive, Inc.
6959257
In Commercial Distribution

  • 00887517704993 ()


  • Spinal implant trial
BASE HL Trial, 12x42x32mm 20°
Nuvasive, Inc.
6959206
In Commercial Distribution

  • 00887517704481 ()


  • Spinal implant trial
BASE HL Trial, 10x42x32mm 20°
Nuvasive, Inc.
6959205
In Commercial Distribution

  • 00887517704474 ()


  • Spinal implant trial
BASE HL Trial, 8x42x32mm 20°
Nuvasive, Inc.
6959204
In Commercial Distribution

  • 00887517704467 ()


  • Spinal implant trial
BASE HL Trial, 6x42x32mm 20°
Nuvasive, Inc.
6959203
In Commercial Distribution

  • 00887517704450 ()


  • Spinal implant trial
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