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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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L-LINE RASPATORY, SLIGHTLY CURVED; 5 MM
Peter Lazic GmbH
46.202
In Commercial Distribution

  • 04250603713296 ()
46.202

  • Open-surgery dissector
L-LINE POLYTOM KNIFE 5 MM; RED
Peter Lazic GmbH
46.191
In Commercial Distribution

  • 04250603713265 ()
46.191

  • Scalpel, reusable
Ear Speculum by Hartmann size 5
FENTEX medical GmbH
018105FX
In Commercial Distribution

  • 04250407700614 ()
018105FX

  • Ear speculum, reusable
Eustachian Catheter by Hartmann size 5
FENTEX medical GmbH
016105FX
In Commercial Distribution

  • 04250407700485 ()
016105FX

  • Eustachian catheter, reusable
straight, 4:5 teeth 14.5 cm
Spiggle & Theis Medizintechnik GmbH
80-401-14
In Commercial Distribution

  • 04250381891490 ()
80-401-14

  • Surgical soft-tissue manipulation forceps, scissors-like, reusable
straight, 4:5 teeth 15.5 cm
Spiggle & Theis Medizintechnik GmbH
80-400-15
In Commercial Distribution

  • 04250381891483 ()
80-400-15

  • Surgical soft-tissue manipulation forceps, scissors-like, reusable
TELIX K Ti Cage 17x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1736
In Commercial Distribution

  • 04250869607872 ()
109-015-1736

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 15x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1536
In Commercial Distribution

  • 04250869607858 ()
109-015-1536

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 13x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1336
In Commercial Distribution

  • 04250869607834 ()
109-015-1336

  • Metallic spinal interbody fusion cage
TELIX K Ti Cage 12x36mm 5°
Biedermann Motech GmbH & Co. KG
109-015-1236
In Commercial Distribution

  • 04250869607827 ()
109-015-1236

  • Metallic spinal interbody fusion cage
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