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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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Trial, H 11mm, 20°, S
EIT Emerging Implant Technologies GmbH
AET71134
In Commercial Distribution

  • 04260397089422 ()


  • Spinal implant trial
THREADED TIP NITINOL GUIDEWIRE 20"
ALPHATEC SPINE, INC.
73770-20-3
In Commercial Distribution

  • 00844856057661 ()


  • Spinal guidewire
BLUNT TIP NITINOL GUIDEWIRE 20"
ALPHATEC SPINE, INC.
73770-20-2
In Commercial Distribution

  • 00844856057654 ()


  • Spinal guidewire
TROCAR TIP NITINOL GUIDEWIRE 20"
ALPHATEC SPINE, INC.
73770-20-1
In Commercial Distribution

  • 00844856057647 ()


  • Spinal guidewire
NERVE ROOT RETRACTOR, 20°, XXL
ALPHATEC SPINE, INC.
27232-05
In Commercial Distribution

  • 00844856081314 ()


  • Hand-held surgical retractor, reusable
NERVE ROOT RETRACTOR, 20°, XL
ALPHATEC SPINE, INC.
27232-04
In Commercial Distribution

  • 00844856081307 ()


  • Hand-held surgical retractor, reusable
NERVE ROOT RETRACTOR, 20°, LARGE
ALPHATEC SPINE, INC.
27232-03
In Commercial Distribution

  • 00844856081291 ()


  • Hand-held surgical retractor, reusable
NERVE ROOT RETRACTOR, 20°, MEDIUM
ALPHATEC SPINE, INC.
27232-02
In Commercial Distribution

  • 00844856081284 ()


  • Hand-held surgical retractor, reusable
NERVE ROOT RETRACTOR, 20°, SMALL
ALPHATEC SPINE, INC.
27232-01
In Commercial Distribution

  • 00844856081277 ()


  • Hand-held surgical retractor, reusable
RACP Single Level Plate, 20
VY SPINE LLC
4-01-020
In Commercial Distribution

  • 00842566103074 ()
4-01-020

  • Spinal fixation plate, non-bioabsorbable
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