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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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LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2414
In Commercial Distribution

  • 08800017217680 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2413
In Commercial Distribution

  • 08800017217673 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2412
In Commercial Distribution

  • 08800017217666 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2411
In Commercial Distribution

  • 08800017217659 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2410
In Commercial Distribution

  • 08800017217642 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2409
In Commercial Distribution

  • 08800017217635 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3516
In Commercial Distribution

  • 08800017217628 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3515
In Commercial Distribution

  • 08800017217611 ()


  • Polymeric spinal interbody fusion cage
MODIFIED INSTRUMENT BENDER TIP, B 20 DEGREES
DEPUY SPINE, LLC
698335411
In Commercial Distribution

  • 10705034371153 ()
698335411

  • Manual orthopaedic bender, reusable
MODIFIED INSTRUMENT BENDER TIP, B 10 DEGREES
DEPUY SPINE, LLC
698335410
In Commercial Distribution

  • 10705034371146 ()
698335410

  • Manual orthopaedic bender, reusable
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