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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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20 GA Bullet Endoilluminator
Alcon Laboratories, Inc.
8065750974
Not in Commercial Distribution

  • 10380657509741 ()
  • 00380657509744 ()

  • 20 Gauge


  • Ophthalmic laser system beam guide
20 GA Fragmentation Pak
Alcon Laboratories, Inc.
8065750958
In Commercial Distribution

  • 10380657509581 ()
  • 00380657509584 ()

  • 20 Gauge


  • Ophthalmic surgical procedure kit, non-medicated, single-use
20 GA StraightLaser Probe
Alcon Laboratories, Inc.
8065-6786-10
Not in Commercial Distribution

  • 10380656786105 ()
  • 00380656786108 ()

  • 20 Gauge


  • Extracorporeal ultrasound imaging transducer, hand-held
angled, serrated 20 cm
Spiggle & Theis Medizintechnik GmbH
80-468-21
In Commercial Distribution

  • 04250381891780 ()
80-468-21

  • General-purpose surgical scissors, reusable
straight WL 20 cm
Spiggle & Theis Medizintechnik GmbH
50-232-23
In Commercial Distribution

  • 04250381862629 ()
50-232-23

  • ENT probe, reusable
straight, blunt 20 cm
Spiggle & Theis Medizintechnik GmbH
20-612-20
In Commercial Distribution

  • 04250381853641 ()
20-612-20

  • Nasal scissors
size 1 20 cm
Spiggle & Theis Medizintechnik GmbH
10-406-01
In Commercial Distribution

  • 04250381846384 ()
10-406-01

  • Endaural surgical curette, reusable
size 00 20 cm
Spiggle & Theis Medizintechnik GmbH
10-406-20
In Commercial Distribution

  • 04250381846360 ()
10-406-20

  • Endaural surgical curette, reusable
size 000 20 cm
Spiggle & Theis Medizintechnik GmbH
10-406-30
In Commercial Distribution

  • 04250381846353 ()
10-406-30

  • Endaural surgical curette, reusable
TAPERED DRIVER SIZE 20
Evolution Spine LLC
110-A012
In Commercial Distribution

  • 00195860020357 ()
110-A012

  • Orthopaedic implant driver
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