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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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Ring curette, ID 3mm, distally curved
Karl Storz GmbH & Co. KG
28164RB
In Commercial Distribution

  • 04048551106266 ()


  • Open-surgery dissector
Ring curette, ID 5mm, distally curved
Karl Storz GmbH & Co. KG
28164RA
In Commercial Distribution

  • 04048551106259 ()


  • Open-surgery dissector
MAXFRAME(TM) STRUT ID PLUG SET
Synthes GmbH
03.312.821
In Commercial Distribution

  • H679033128210 ()
  • 10886982260994 ()
03312821

  • External orthopaedic fixation system, reusable
MAXFRAME(TM) STRUT ID BAND SET
Synthes GmbH
03.312.820
In Commercial Distribution

  • H679033128200 ()
  • 10886982260987 ()
03312820

  • External orthopaedic fixation system, reusable
DETACHAB. INSTRUMENT PORT ID 8.5MM reusable
Richard Wolf GmbH
8911316
Not in Commercial Distribution

  • 04055207021910 ()

  • Lumen/Inner Diameter: 8.5 Millimeter
8911.316

  • Pin-indexed adaptor, reusable
Metal ID Tag for Container - Blue
FLEXBAR MACHINE CORPORATION
72245M
In Commercial Distribution

  • 00842102104886 ()
72245M

  • Device sterilization/disinfection container, reusable
Bencox ID stem Rasp No.11
Corentec Co., Ltd
01.55.011
In Commercial Distribution

  • 08806373888748 ()


  • Femoral stem prosthesis trial
  • Bone file/rasp, manual, reusable
Bencox ID stem Rasp No.10
Corentec Co., Ltd
01.55.010
In Commercial Distribution

  • 08806373888731 ()


  • Bone file/rasp, manual, reusable
  • Femoral stem prosthesis trial
Bencox ID stem Rasp No.9
Corentec Co., Ltd
01.55.009
In Commercial Distribution

  • 08806373888724 ()


  • Femoral stem prosthesis trial
  • Bone file/rasp, manual, reusable
Bencox ID stem Rasp No.8
Corentec Co., Ltd
01.55.008
In Commercial Distribution

  • 08806373888717 ()


  • Bone file/rasp, manual, reusable
  • Femoral stem prosthesis trial
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