SEARCH RESULTS FOR: (*purchase Wyoming driver*)(3010 results)

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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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NA - 10887587049267

1.0MM TI MEDIAL WALL PLATE RIGHT-STERILE
Synthes GmbH
420.45S
In Commercial Distribution

  • H98042045S0 ()
  • 10887587049267 ()
42045S

  • Craniofacial fixation plate, non-bioabsorbable, non-customized

NA - 10887587024578

BATTERY PACK-STERILE FOR BATTERY POWERED DRIVER
Synthes GmbH
05.000.007.01S
In Commercial Distribution

  • H9800500000701S0 ()
  • 10887587024578 ()
0500000701S

  • Secondary battery

MatrixMIDFACE - 10887587023175

TI MATRIXMIDFACE PREFORMED ORBITAL PLATE LARGE/RIGHT-STER
Synthes GmbH
04.503.812S
In Commercial Distribution

  • H98004503812S0 ()
  • 10887587023175 ()
04503812S

  • Craniofacial fixation plate, non-bioabsorbable, non-customized

MatrixMIDFACE - 10887587023151

TI MATRIXMIDFACE PREFORMED ORBITAL PLATE SMALL/RIGHT-STER
Synthes GmbH
04.503.811S
In Commercial Distribution

  • H98004503811S0 ()
  • 10887587023151 ()
04503811S

  • Craniofacial fixation plate, non-bioabsorbable, non-customized

MatrixMIDFACE - 10887587023137

TI MATRIXMIDFACE PREFORMED ORBITAL PLATE LARGE/LEFT-STER
Synthes GmbH
04.503.802S
In Commercial Distribution

  • H98004503802S0 ()
  • 10887587023137 ()
04503802S

  • Craniofacial fixation plate, non-bioabsorbable, non-customized

MatrixMIDFACE - 10887587023113

TI MATRIXMIDFACE PREFORMED ORBITAL PLATE SMALL/LEFT-STER
Synthes GmbH
04.503.801S
In Commercial Distribution

  • H98004503801S0 ()
  • 10887587023113 ()
04503801S

  • Craniofacial fixation plate, non-bioabsorbable, non-customized

Fixone Biocomposite Anchor - 08806109701068

The Fixone Biocomposite Anchor is intended for reattaching soft tissue to bone with sutures. The anchor ismanufactured from biodegradable materials (PLGA copolymer and beta-TCP). A nonabsorbable UHMWPE suture is inserted into the anchor. The anchor is implanted using a provided driver. B,N,BN type(Knotted suture anchors) are ‘screw-in’ anchors used alone or in combination with Kc,KcN type(Knotless suture anchors) for soft-tissue repair. Kc,KcN type(Knotless suture anchor) are used for a soft-tissue repair in combination with the B,N,BN type. SL type ‘push-in’ anchors that are ideal for soft-tissue repair in narrow or deep areas. S type are ‘push-in’ anchors that are ideal for soft-tissue repair in the foot, ankle, hand and wrist The Fixone Biocomposite Anchor consists of cannulated anchors with an eyelet. They are pre-loaded on an insertion device. The Fixone Biocomposite Anchor is intended to provide secure reattachment of the soft tissue to bone. Devices are provided sterile. Single use only.
AJU PHARM. CO., LTD.
SAB-30002e
In Commercial Distribution

  • 08806109701068 ()


  • Tendon/ligament bone anchor, bioabsorbable

NA - 10886982347572

RFN-ADVANCED POLYMER INLAY STERILE
Synthes GmbH
08.233.001S
In Commercial Distribution

  • 10886982347572 ()
08233001S

  • Bone screw fixation sleeve

OsteoMed - 00845694094894

1.8mm Cannulated Drill, Sterile, Qty 5
OSTEOMED LLC
320-5218-SP-05
In Commercial Distribution

  • 00845694094894 ()

  • Length: 116 Millimeter
320-5218-SP-05

  • Cannulated surgical drill bit, single-use

OsteoMed - 00845694094887

1.8mm Cannulated Drill, Sterile, Qty 2
OSTEOMED LLC
320-5218-SP-02
In Commercial Distribution

  • 00845694094887 ()

  • Length: 116 Millimeter
320-5218-SP-02

  • Cannulated surgical drill bit, single-use
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