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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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FORCEPS WITH WINDOW/SPIKE
HOYA CORPORATION
KH2422S
Not in Commercial Distribution

  • 04961333224784 ()
  • 04961333072927 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW/SPIKE
HOYA CORPORATION
KH2415S
Not in Commercial Distribution

  • 04961333224746 ()
  • 04961333071036 ()


  • Open-surgery biopsy forceps, reusable
FORCEPS WITH WINDOW/SPIKE
HOYA CORPORATION
KH2411S
Not in Commercial Distribution

  • 04961333224722 ()
  • 04961333083473 ()


  • Open-surgery biopsy forceps, reusable
Cysto-Urethroscope Sheath with obtu
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
32-4092
In Commercial Distribution

  • 00848657019606 ()


  • Endoscope sheath, reusable
Cysto-Urethroscope Sheath with obtu
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
32-4087
In Commercial Distribution

  • 00848657019590 ()


  • Endoscope sheath, reusable
Cysto-Urethroscope Sheath with obtu
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
32-4077
In Commercial Distribution

  • 00848657019576 ()


  • Endoscope sheath, reusable
with Rectal Flap, 6F
Laborie Medical Technologies Canada ULC
9021T1061
In Commercial Distribution

  • 10627825007426 ()
  • 00627825007412 ()


  • Urodynamic manometric catheter, non-electronic
with Rectal Flap, 8F
Laborie Medical Technologies Canada ULC
9021T1031
In Commercial Distribution

  • 10627825007334 ()
  • 00627825007320 ()


  • Urodynamic manometric catheter, non-electronic
Cysto-Urethroscope Sheath with obtu
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
32-4082
In Commercial Distribution

  • 00848657019583 ()


  • Endoscope sheath, reusable
Cysto-Urethroscope Sheath with obtu
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
32-4072
In Commercial Distribution

  • 00848657019569 ()


  • Endoscope sheath, reusable
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