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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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NA - 04715309124765

"Measure uterine depth. Dilate the cervix if necessary. Introduce INTRACURETTE through the cervical canal into the uterus up to the fundus. Connect the curette to the suction system. Operate by rotating the curette 360∘ to aspirate throughout the uterus cavity accurately. Repeat the operation two or three times. Withdraw INTRACURETTE from the uterus while continuing the rotating movement. "
PANPAC MEDICAL CORPORATION
CuRs07
In Commercial Distribution

  • 04715309125281 ()
  • 04715309124765 ()


  • Intrauterine curette, suction

NA - 04715309124840

"Measure uterine depth. Dilate the cervix if necessary. Introduce INTRACURETTE through the cervical canal into the uterus up to the fundus. Connect the curette to the suction system. Operate by rotating the curette 360∘ to aspirate throughout the uterus cavity accurately. Repeat the operation two or three times. Withdraw INTRACURETTE from the uterus while continuing the rotating movement. "
PANPAC MEDICAL CORPORATION
CuRc08
In Commercial Distribution

  • 04715309125366 ()
  • 04715309124840 ()


  • Intrauterine curette, suction

NA - 04715309124796

"Measure uterine depth. Dilate the cervix if necessary. Introduce INTRACURETTE through the cervical canal into the uterus up to the fundus. Connect the curette to the suction system. Operate by rotating the curette 360∘ to aspirate throughout the uterus cavity accurately. Repeat the operation two or three times. Withdraw INTRACURETTE from the uterus while continuing the rotating movement. "
PANPAC MEDICAL CORPORATION
CuRs10
In Commercial Distribution

  • 04715309124796 ()


  • Intrauterine curette, suction

NA - 04715309124772

"Measure uterine depth. Dilate the cervix if necessary. Introduce INTRACURETTE through the cervical canal into the uterus up to the fundus. Connect the curette to the suction system. Operate by rotating the curette 360∘ to aspirate throughout the uterus cavity accurately. Repeat the operation two or three times. Withdraw INTRACURETTE from the uterus while continuing the rotating movement. "
PANPAC MEDICAL CORPORATION
CuRs08
In Commercial Distribution

  • 04715309125298 ()
  • 04715309124772 ()


  • Intrauterine curette, suction

NA - 04715309124758

"Measure uterine depth. Dilate the cervix if necessary. Introduce INTRACURETTE through the cervical canal into the uterus up to the fundus. Connect the curette to the suction system. Operate by rotating the curette 360∘ to aspirate throughout the uterus cavity accurately. Repeat the operation two or three times. Withdraw INTRACURETTE from the uterus while continuing the rotating movement. "
PANPAC MEDICAL CORPORATION
CuRs06
In Commercial Distribution

  • 04715309125274 ()
  • 04715309124758 ()


  • Intrauterine curette, suction

VERTEX® Reconstruction System - 00613994514493

ROD 7755123 3.2MM/3.5MM X 220 OCCIP ADJ
MEDTRONIC SOFAMOR DANEK, INC.
7755123
In Commercial Distribution

  • 00613994514493 ()

  • Length: 220.0 Millimeter
  • 3.2 to 3.5MM


  • Bone-screw internal spinal fixation system rod

Atoll - 10889981033767

Wedding Band 5.5mm to 3.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-5550
In Commercial Distribution

  • 10889981033767 ()

  • 5.5mm to 3.5mm
16-23-5550

  • Bone-screw internal spinal fixation system connector

Atoll - 10889981033750

Slimline 3.5mm to 5.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-5540
In Commercial Distribution

  • 10889981033750 ()

  • 3.5mm to 5.5mm
16-23-5540

  • Bone-screw internal spinal fixation system connector

Atoll - 10889981033743

Clamshell 3.5mm to 5.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-5530
In Commercial Distribution

  • 10889981033743 ()

  • 3.5mm to 5.5mm
16-23-5530

  • Bone-screw internal spinal fixation system connector

Atoll - 10889981033736

Inline 3.5mm to 5.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-5520
In Commercial Distribution

  • 10889981033736 ()

  • 3.5mm to 5.5mm
16-23-5520

  • Bone-screw internal spinal fixation system, non-sterile

Atoll - 10889981033729

Offset 5.5mm to 3.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-5510
In Commercial Distribution

  • 10889981033729 ()

  • 5.5mm to 3.5mm
16-23-5510

  • Bone-screw internal spinal fixation system connector

Atoll - 10889981033712

Clamshell 3.5mm to 3.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-3530
Not in Commercial Distribution

  • 10889981033712 ()

  • 3.5mm to 3.5mm
16-23-3530

  • Bone-screw internal spinal fixation system connector

Atoll - 10889981033705

Wedding Band 3.5mm to 3.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-3520
In Commercial Distribution

  • 10889981033705 ()

  • 3.5mm to 3.5mm
16-23-3520

  • Bone-screw internal spinal fixation system connector

Atoll - 10889981033699

Offset 3.5mm to 3.5mm Connector Asm. The Atoll OCT Spinal System is intended for use as an aid in spine fusion. It consists of screws, hooks, rods, and connectors. These components are available in a variety of sizes to allow for a variety of configurations to better fit each individual patient's pathology. The Atoll OCT Spinal System components are manufactured from medical implant grade titanium alloy Ti-6Al-4V (ELI) per ASTM F-136 or ISO 5832-3.
Seaspine Orthopedics Corporation
16-23-3510
In Commercial Distribution

  • 10889981033699 ()

  • 3.5mm to 3.5mm
16-23-3510

  • Bone-screw internal spinal fixation system connector

Coral - 10889981030209

Inline Connector, 5.5mm to 5.5mm
Seaspine Orthopedics Corporation
10-23-0130
In Commercial Distribution

  • 10889981030209 ()

  • 5.5mm to 5.5mm
10-23-0130

  • Bone-screw internal spinal fixation system, non-sterile

Coral - 10889981030193

Clamshell Connector, 5.5mm to 5.5mm
Seaspine Orthopedics Corporation
10-23-0120
In Commercial Distribution

  • 10889981030193 ()

  • 5.5mm to 5.5mm
10-23-0120

  • Bone-screw internal spinal fixation system connector

Coral - 10889981030186

Wedding Band Connector, 5.5mm to 5.5mm
Seaspine Orthopedics Corporation
10-23-0110
In Commercial Distribution

  • 10889981030186 ()

  • 5.5mm to 5.5mm
10-23-0110

  • Bone-screw internal spinal fixation system connector

Coral - 10889981030179

Domino Connector, 5.5mm to 5.5mm
Seaspine Orthopedics Corporation
10-23-0100
In Commercial Distribution

  • 10889981030179 ()

  • 5.5mm to 5.5mm
10-23-0100

  • Bone-screw internal spinal fixation system connector

EXACT CYLINDRICAL REAMER - 00880304396784

No Description
Biomet Orthopedics, LLC
595099
In Commercial Distribution

  • 00880304396784 ()

  • 8MM TO 20MM
595099

  • Instrument tray, reusable

ROMEO Posterior Osteosynthesis system - 07640151084561

Cross Connector / Multiaxial Prebent
SpineArt SA
ELL-CC MP 55-S
In Commercial Distribution

  • 07640151084561 ()

  • L55 to 80


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084547

Cross Connector / Multiaxial Prebent
SpineArt SA
ELL-CC MP 43-S
In Commercial Distribution

  • 07640151084547 ()

  • L43 to 55


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084523

Cross Connector / Multiaxial Prebent
SpineArt SA
ELL-CC MP 36-S
In Commercial Distribution

  • 07640151084523 ()

  • L36 to 43


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084509

Cross Connector / Multiaxial Prebent
SpineArt SA
ELL-CC MP 33-S
In Commercial Distribution

  • 07640151084509 ()

  • L33 to L36


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084073

Cross Connector / Multiaxial
SpineArt SA
ELL-CC MU 43-S
In Commercial Distribution

  • 07640151084073 ()

  • L43 to 55


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084066

Cross Connector / Multiaxial
SpineArt SA
ELL-CC MU 36-S
In Commercial Distribution

  • 07640151084066 ()

  • L36 to 43


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084059

Cross Connector / Multiaxial
SpineArt SA
ELL-CC MU 33-S
In Commercial Distribution

  • 07640151084059 ()

  • L33 to 36


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084042

Cross Connector / Multiaxial
SpineArt SA
ELL-CC MU 31-S
In Commercial Distribution

  • 07640151084042 ()

  • L31 to 33


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151084035

Cross Connector / Multiaxial
SpineArt SA
ELL-CC MU 30-S
In Commercial Distribution

  • 07640151084035 ()

  • L30 to 31


  • Bone-screw internal spinal fixation system, sterile

ROMEO Posterior Osteosynthesis system - 07640151082512

Cross Connector / Multiaxial
SpineArt SA
ELL-CC MU 55-S
In Commercial Distribution

  • 07640151082512 ()

  • L55 to 80


  • Bone-screw internal spinal fixation system, sterile

MEDENTiKA - EMKA809

MedentiBASE Laboratory implant
MEDENTiKA GmbH
80
In Commercial Distribution

  • 04251574837455 ()
  • EMKA809 ()

  • compatible to MedentiBase
80

  • Dental implant analog

MEDENTiKA - EMKA599

Novaloc
MEDENTiKA GmbH
59
In Commercial Distribution

  • 04251574805836 ()
  • EMKA599 ()

  • compatible to Novaloc
59

  • Dental implant analog

MEDENTiKA - EMKA589

Novaloc
MEDENTiKA GmbH
58
In Commercial Distribution

  • 04251574805829 ()
  • EMKA589 ()

  • compatible to Novaloc
58

  • Dental implant analog

MEDENTiKA - EMKA579

MedentiLOC
MEDENTiKA GmbH
57
In Commercial Distribution

  • 04251574805812 ()
  • EMKA579 ()

  • compatible to MedentiLOC
57

  • Dental implant analog

MEDENTiKA - EMKA569

MedentiLOC
MEDENTiKA GmbH
56
In Commercial Distribution

  • 04251574805805 ()
  • EMKA569 ()

  • compatible to MedentiLOC
56

  • Dental implant analog

MEDENTiKA - EMKA46309

MedentiBASE Laboratory implant
MEDENTiKA GmbH
4630
In Commercial Distribution

  • 04251574805768 ()
  • EMKA46309 ()

  • compatible to MedentiBase
4630

  • Dental implant analog

MEDENTiKA - EMKA8515309

Multi-unit Laboratory implant
MEDENTiKA GmbH
8515-30
In Commercial Distribution

  • 04251574835093 ()
  • EMKA8515309 ()

  • compatible to Multi-unit
8515-30

  • Dental implant analog

MEDENTiKA - EMKA8515179

Multi-unit Laboratory implant
MEDENTiKA GmbH
8515-17
In Commercial Distribution

  • 04251574835086 ()
  • EMKA8515179 ()

  • compatible to Multi-unit
8515-17

  • Dental implant analog

MEDENTiKA - EMKA8514309

Multi-unit Laboratory implant
MEDENTiKA GmbH
8514-30
In Commercial Distribution

  • 04251574805881 ()
  • EMKA8514309 ()

  • compatible to Multi-unit
8514-30

  • Dental implant analog

MEDENTiKA - EMKA8514179

Multi-unit Laboratory implant
MEDENTiKA GmbH
8514-17
In Commercial Distribution

  • 04251574805874 ()
  • EMKA8514179 ()

  • compatible to Multi-unit
8514-17

  • Dental implant analog

MEDENTiKA - EMKA85109

Multi-unit Laboratory implant
MEDENTiKA GmbH
8510
In Commercial Distribution

  • 04251574805867 ()
  • EMKA85109 ()

  • compatible to Multi-unit
8510

  • Dental implant analog
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