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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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Sun-Schein Syringe 55 Dark
HENRY SCHEIN, INC.
1005894
In Commercial Distribution

  • 00304040002339 ()
1005894

  • Dental composite resin
Sun-Schein Syringe 67 Light
HENRY SCHEIN, INC.
1005607
In Commercial Distribution

  • 00304040002315 ()
1005607

  • Dental composite resin
Veneer Cement Refill Syringe
HENRY SCHEIN, INC.
1005216
In Commercial Distribution

  • 00304040002308 ()
1005216

  • Dental composite resin
Sun-Schein Syringe 59 Light
HENRY SCHEIN, INC.
1005056
In Commercial Distribution

  • 00304040002292 ()
1005056

  • Dental composite resin
Sun-Schein Introductory
HENRY SCHEIN, INC.
1002124
In Commercial Distribution

  • 00304040002285 ()
1002124

  • Dental composite resin
Veneer Cement Refill Syringe
HENRY SCHEIN, INC.
1005217
In Commercial Distribution

  • 00304040024003 ()
1005217

  • Dental composite resin
Veneer Cement Refill Syringe
HENRY SCHEIN, INC.
1009906
In Commercial Distribution

  • 00304040023990 ()
1009906

  • Dental composite resin
Veneer Cement Refill Syringe
HENRY SCHEIN, INC.
1009350
In Commercial Distribution

  • 00304040023983 ()
1009350

  • Dental composite resin
No Description
MAXTEC, LLC
R500P21
Not in Commercial Distribution

  • 10817770020810 ()


  • Exhaled-gas oesophageal intubation detector
The Drivewire 24 Guidewire is a 0.024” steerable guidewire with a deflectable tip controlled via a proximal handle. The distal section is radiopaque to aid fluoroscopic visualization and has a hydrophilic polymer coating. The guidewire packaging includes a torque device.
RAPID MEDICAL LTD
DRPP2411
In Commercial Distribution

  • 07290015107358 ()


  • Cardiac/peripheral vascular guidewire, single-use
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