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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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BLINK MEDICAL LIMITED
HR500
In Commercial Distribution

  • 05060480406193 ()
  • 05060480400658 ()


  • Suturing needle holder, single-use
Basket Cannula Distal Tip for ID:2.5mm, OD:3.0mm, Basket Cannula Tube ID:2.5mm, OD:3.0mm
Extremity Care
ALC425
In Commercial Distribution

  • 00850003042381 ()


  • Tissue injection cannula
Cobra Cannula Distal Tip for ID:2.5mm, OD:3.0mm, Spatula & Cobra Cannula Tube ID:2.5mm, OD:3.0mm
Extremity Care
ALC325
In Commercial Distribution

  • 00850003042282 ()

  • Outer Diameter: 3 Millimeter


  • Tissue injection cannula
Spatula Cannula Distal Tip for ID:2.5mm, OD:3.0mm, Spatula & Cobra Cannula Tube ID:2.5mm, OD:3.0mm
Extremity Care
ALC225
In Commercial Distribution

  • 00850003042275 ()

  • Outer Diameter: 3 Millimeter


  • Tissue injection cannula
Straight Cannula Distal Tip for ID:2.5mm, OD:3.0mm, Straight Cannula Tube ID:2.5mm, OD:3.0mm
Extremity Care
ALC125
In Commercial Distribution

  • 00850003042268 ()


  • Tissue injection cannula
STERILE 6 CRILE WOOD NDL HLDR
MEDLINE INDUSTRIES, INC.
DYND04111
In Commercial Distribution

  • 40888277293848 ()
  • 10888277293847 ()
DYND04111

  • Suturing needle holder, single-use
STERILE WBSTR NDL HLDR SATIN
MEDLINE INDUSTRIES, INC.
DYND04105
In Commercial Distribution

  • 40888277293367 ()
  • 10888277293366 ()
DYND04105

  • Suturing needle holder, single-use
2.4MM THREADED REDUCTION TOOL SELF-DRILLING 78MM HEX-STERILE
Synthes GmbH
03.507.002S
In Commercial Distribution

  • H98003507002S0 ()
  • 10887587014166 ()
03507002S

  • Orthopaedic bone-fragment manipulator, single-use
PUSH PIN
KLS-Martin L.P.
25-408-01-75
In Commercial Distribution

  • 10888118039993 ()
  • 00888118039996 ()


  • Suturing needle holder, single-use
PREPIDIL Gel is available as a sterile semitranslucent viscous preparation for endocervical application: 0.5 mg PGE2 per 3.0 g (2.5 mL) in syringe. In addition, each package contains two shielded catheters (10 mm and 20 mm tip) enclosed in sterile envelopes. The contents are not guaranteed sterile if envelopes are not intact.
PHARMACIA & UPJOHN COMPANY LLC
NDC 0009-3359-01
In Commercial Distribution

  • 00300093359024 ()
  • 00300093359017 ()


  • Cervical dilatation catheter
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