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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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CUP CURETTE, STRAIGHT, UP, 10°, SERRATED
HYHTE HOLDINGS, INC.
GZB13S105
In Commercial Distribution

  • 00840085201547 ()

  • 5
GZB13S105

  • Bone curette, reusable
CUP CURETTE, STRAIGHT, UP, 10°, SERRATED
HYHTE HOLDINGS, INC.
GZB13S104
In Commercial Distribution

  • 00840085201530 ()

  • 4
GZB13S104

  • Bone curette, reusable
CUP CURETTE, STRAIGHT, UP, 10°, SERRATED
HYHTE HOLDINGS, INC.
GZB13S103
In Commercial Distribution

  • 00840085201523 ()

  • 3
GZB13S103

  • Bone curette, reusable
CUP CURETTE, STRAIGHT, UP, 10°
HYHTE HOLDINGS, INC.
GZB13S006
In Commercial Distribution

  • 00840085201493 ()

  • 6
GZB13S006

  • Bone curette, reusable
CUP CURETTE, STRAIGHT, UP, 10°
HYHTE HOLDINGS, INC.
GZB13S004
In Commercial Distribution

  • 00840085201479 ()

  • 4
GZB13S004

  • Bone curette, reusable
CUP CURETTE, STRAIGHT, UP, 10°
HYHTE HOLDINGS, INC.
GZB13S003
In Commercial Distribution

  • 00840085201462 ()

  • 3
GZB13S003

  • Bone curette, reusable
LONG CANNULATED REAMER 4.8MM OD X 1.8MM ID
Smith & Nephew, Inc.
71010006
In Commercial Distribution

  • 03596010442239 ()
71010006

  • Bone-resection orthopaedic reamer, reusable
GENESIS II POSTERIOR STABILIZED CONSTRAINED HOUSING REAMER DOME
Smith & Nephew, Inc.
71440145
In Commercial Distribution

  • 03596010471338 ()
71440145

  • Bone-resection orthopaedic reamer, reusable
GENESIS II MODIFIED BICONVEX PATELLAR REAMER 23MM
Smith & Nephew, Inc.
71440634
In Commercial Distribution

  • 03596010463524 ()
71440634

  • Bone-resection orthopaedic reamer, reusable
GENESIS II MODIFIED BICONVEX PATELLAR REAMER 32MM
Smith & Nephew, Inc.
71440640
In Commercial Distribution

  • 03596010464897 ()
71440640

  • Bone-resection orthopaedic reamer, reusable
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