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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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Augmented VaultLock® Reamer, Locking, M
ARTHREX, INC.
AR-9275T-M
In Commercial Distribution

  • 00888867498990 ()
AR-9275T-M

  • Bone-resection orthopaedic reamer, single-use
Augmented VaultLock® Reamer, Locking, L
ARTHREX, INC.
AR-9275T-L
In Commercial Distribution

  • 00888867498983 ()
AR-9275T-L

  • Bone-resection orthopaedic reamer, single-use
VIP™ Augmented MGS Reamer, Locking, S
ARTHREX, INC.
AR-5410T-AMGS-S
In Commercial Distribution

  • 00888867498976 ()
AR-5410T-AMGS-S

  • Bone-resection orthopaedic reamer, single-use
VIP™ Augmented MGS Reamer, Locking, M
ARTHREX, INC.
AR-5410T-AMGS-M
In Commercial Distribution

  • 00888867498969 ()
AR-5410T-AMGS-M

  • Bone-resection orthopaedic reamer, single-use
VIP™ Augmented MGS Reamer, Locking, L
ARTHREX, INC.
AR-5410T-AMGS-L
In Commercial Distribution

  • 00888867498952 ()
AR-5410T-AMGS-L

  • Bone-resection orthopaedic reamer, single-use
Polypectomy Snare, Stiff Wire
ENDOCHOICE, INC.
DSO-013
Not in Commercial Distribution

  • 00816849017600 ()
  • 00816849017594 ()


  • Polypectomy endoscopic ligator, single-use
Anti-Rotation Bar, Long, Strl
ARTHREX, INC.
AR-9095-67LS
In Commercial Distribution

  • 00888867458154 ()
AR-9095-67LS

  • Bone lever/elevator, single-use
Anti-Rotation Bar, Short, Strl
ARTHREX, INC.
AR-9095-67S
In Commercial Distribution

  • 00888867430495 ()
AR-9095-67S

  • Bone lever/elevator, single-use
Cage Bent Curette Kit
Neo Medical SA
CI-00-BC-00
In Commercial Distribution

  • 07640177822017 ()


  • Bone curette, single-use
Cage straight curette kit XL
Neo Medical SA
CI-00-SC-XL
In Commercial Distribution

  • 07640177822352 ()


  • Bone curette, single-use
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