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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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Origin Hip Stem - 09348215051570

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1201
In Commercial Distribution

  • 09348215051570 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051563

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1101
In Commercial Distribution

  • 09348215051563 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051556

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1001
In Commercial Distribution

  • 09348215051556 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051549

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-0901
In Commercial Distribution

  • 09348215051549 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051532

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1800
In Commercial Distribution

  • 09348215051532 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051525

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1600
In Commercial Distribution

  • 09348215051525 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051518

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1500
In Commercial Distribution

  • 09348215051518 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051501

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1400
In Commercial Distribution

  • 09348215051501 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051495

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1300
In Commercial Distribution

  • 09348215051495 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051488

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1200
In Commercial Distribution

  • 09348215051488 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051471

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1100
In Commercial Distribution

  • 09348215051471 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051464

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-1000
In Commercial Distribution

  • 09348215051464 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051457

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-0900
In Commercial Distribution

  • 09348215051457 ()


  • Coated femoral stem prosthesis, modular

Origin Hip Stem - 09348215051440

No Description
SIGNATURE ORTHOPAEDICS PTY LTD
D111-18-0800
In Commercial Distribution

  • 09348215051440 ()


  • Coated femoral stem prosthesis, modular

Avery Breathing Pacemaker System - 00850252006035

(902A) 1.0 m Lead Length
Avery Biomedical Devices Inc
External Antenna
In Commercial Distribution

  • 00850252006035 ()
902A

  • Extramuscular diaphragm/phrenic nerve electrical stimulation system

Avery Breathing Pacemaker System - 00850252006066

Digital Transmitter for the Avery Breathing Pacemaker System
Avery Biomedical Devices Inc
NeurostimulatorTransmitter Digital
In Commercial Distribution

  • 00850252006066 ()
Spirit

  • Extramuscular diaphragm/phrenic nerve electrical stimulation system

Avery Breathing Pacemaker System - 00850252006059

No Description
Avery Biomedical Devices Inc
Transtelephonic Monitor
Not in Commercial Distribution

  • 00850252006059 ()
TTM

  • Extramuscular diaphragm/phrenic nerve electrical stimulation system

Avery Breathing Pacemaker System - 00850252006042

(902A) 2.0 m Lead Length
Avery Biomedical Devices Inc
External Antenna
In Commercial Distribution

  • 00850252006042 ()
902AL

  • Extramuscular diaphragm/phrenic nerve electrical stimulation system

Avery Breathing Pacemaker System - 00850252006004

No Description
Avery Biomedical Devices Inc
Neurostimulator Transmitter
In Commercial Distribution

  • 00850252006004 ()
MARK IV

  • Extramuscular diaphragm/phrenic nerve electrical stimulation system

Epicel (cultured epidermal autografts) - W41020AU201S1969

Epicel (cultured epidermal autografts) is an aseptically processed wound dressing composed of the patient’s own (autologous) keratinocytes grown ex vivo in the presence of proliferation-arrested, murine (mouse) fibroblasts. Epicel consists of sheets of proliferative, autologous keratinocytes, ranging from 2 to 8 cell layers thick and is referred to as a cultured epidermal autograft. Each graft of Epicel is attached to petrolatum gauze backing with titanium surgical clips and measures a minimum of 50 cm2 in area. Epicel is authorized by Federal law for use in adult and pediatric patients who have deep dermal or full-thickness burns comprising a total body surface area greater than or equal to 30%. Epicel may be used in conjunction with split-thickness autografts, or alone in patients for whom split-thickness autografts may not be an option due to the severity and extent of their burns.
VERICEL CORPORATION
N/A
In Commercial Distribution

  • W41020AU201S1969 ()

  • Area/Surface Area: 50 Square centimeter


  • Cultured skin autograft/xenograft

Epicel (cultured epidermal autografts) - W41020AU201P0001

Epicel (cultured epidermal autografts) is an aseptically processed wound dressing composed of the patient’s own (autologous) keratinocytes grown ex vivo in the presence of proliferation-arrested, murine (mouse) fibroblasts. Epicel consists of sheets of proliferative, autologous keratinocytes, ranging from 2 to 8 cell layers thick and is referred to as a cultured epidermal autograft. Each graft of Epicel is attached to petrolatum gauze backing with titanium surgical clips and measures approximately 50 cm2 in area. Epicel is authorized by Federal law for use in adult and pediatric patients who have deep dermal or full-thickness burns comprising a total body surface area greater than or equal to 30%. Epicel may be used in conjunction with split-thickness autografts, or alone in patients for whom split-thickness autografts may not be an option due to the severity and extent of their burns.
VERICEL CORPORATION
0
In Commercial Distribution

  • W41020AU201P0001 ()

  • Area/Surface Area: 50 Square centimeter


  • Cultured skin autograft/xenograft

SYNCHROMED®II - 00643169984226

PUMP 8637-40 SYNCHROMED II 40ML DLC US
MEDTRONIC, INC.
8637-40
In Commercial Distribution

  • 00643169984226 ()

  • Total Volume: 40.0 Milliliter


  • Implantable intrathecal infusion pump, programmable

SYNCHROMED®II - 00643169984219

PUMP 8637-20 SYNCHROMED II 20ML DLC US
MEDTRONIC, INC.
8637-20
In Commercial Distribution

  • 00643169984219 ()

  • Total Volume: 20.0 Milliliter


  • Implantable intrathecal infusion pump, programmable

SYNCHROMED® II - 00643169630512

PUMP 8637-40 SYNCHMED II 40ML EMAN SYMBL
MEDTRONIC, INC.
8637-40
In Commercial Distribution

  • 00643169630512 ()

  • Reservoir Volume 40 mL


  • Implantable intrathecal infusion pump, programmable

SYNCHROMED® II - 00643169630505

PUMP 8637-20 SYNCHMED II 20ML EMAN SYMBL
MEDTRONIC, INC.
8637-20
In Commercial Distribution

  • 00643169630505 ()

  • Reservoir Volume 20 mL


  • Implantable intrathecal infusion pump, programmable

SYNCHROMED® II - 00643169508156

PUMP 8637-40 SYNCHMED II 40ML POTTED FTS
MEDTRONIC, INC.
8637-40
In Commercial Distribution

  • 00643169508156 ()


  • Implantable intrathecal infusion pump, programmable

SYNCHROMED® II - 00643169508149

PUMP 8637-20 SYNCHMED II 20ML POTTED FTS
MEDTRONIC, INC.
8637-20
In Commercial Distribution

  • 00643169508149 ()


  • Implantable intrathecal infusion pump, programmable

SynchroMed® II - 00643169530126

PUMP 8637-40 SYNCHMED II 40ML DLC MOTOR
MEDTRONIC, INC.
8637-40
In Commercial Distribution

  • 00643169530126 ()

  • Total Volume: 40.0 Milliliter


  • Implantable intrathecal infusion pump, programmable

SynchroMed® II - 00643169530119

PUMP 8637-20 SYNCHMED II 20ML DLC MOTOR
MEDTRONIC, INC.
8637-20
In Commercial Distribution

  • 00643169530119 ()

  • Total Volume: 20.0 Milliliter


  • Implantable intrathecal infusion pump, programmable

SYNCHROMED ® II - 00643169100831

PUMP 8637-20 SYNCHMED II 20ML PF
MEDTRONIC, INC.
8637-20
In Commercial Distribution

  • 00643169100831 ()

  • Total Volume: 20.0 Milliliter


  • Implantable intrathecal infusion pump, programmable
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