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Non Sterilized
Bedal
Bedal air M
In Commercial Distribution
- 05430000258487 ()
- Length: 120 Millimeter
- Width: 83.2 Millimeter
- Height: 14.4 Millimeter
DPNS01
- Synthetic polymer semi-permeable film dressing, adhesive
Sterilized
Bedal
bedal air S
In Commercial Distribution
- 05430000258418 ()
- 05430000258401 ()
- 05430000258425 ()
- Length: 78 Millimeter
- Width: 38.8 Millimeter
- Height: 11.1 Millimeter
UN02
- Synthetic polymer semi-permeable film dressing, adhesive
Sterilized
Bedal
bedal flex, epi/pnb
In Commercial Distribution
- 05430000258371 ()
- 05430000258364 ()
- 05430000258388 ()
- Length: 95 Millimeter
- Width: 60 Millimeter
- Height: 6.4 Millimeter
EP02
- Synthetic polymer semi-permeable film dressing, adhesive
Sterilized
Bedal
bedal pivc
In Commercial Distribution
- 05430000258333 ()
- 05430000258326 ()
- 05430000258340 ()
- Length: 70 Millimeter
- Width: 44.8 Millimeter
- Height: 15 Millimeter
PV02
- Synthetic polymer semi-permeable film dressing, adhesive
Sterilized
Bedal
bedal picc/cvc
In Commercial Distribution
- 05430000258210 ()
- 05430000258203 ()
- 05430000258234 ()
- Length: 78 Millimeter
- Width: 38.8 Millimeter
- Height: 10.2 Millimeter
PC02
- Synthetic polymer semi-permeable film dressing, adhesive
Programmer and Software
LIVANOVA USA, INC.
3100
In Commercial Distribution
- 05425025750634 ()
- Vagus nerve electrical stimulation system programmer
Programmer
LIVANOVA USA, INC.
3000
In Commercial Distribution
- 05425025750535 ()
- Vagus nerve electrical stimulation system programmer
Programmer
LIVANOVA USA, INC.
3000
In Commercial Distribution
- 05425025750481 ()
- Vagus nerve electrical stimulation system programmer
Programmer
LIVANOVA USA, INC.
3000
In Commercial Distribution
- 05425025750443 ()
- Vagus nerve electrical stimulation system programmer
Programmer
LIVANOVA USA, INC.
3000
In Commercial Distribution
- 05425025750429 ()
- Vagus nerve electrical stimulation system programmer
Programmer
LIVANOVA USA, INC.
3000
In Commercial Distribution
- 05425025750399 ()
- Vagus nerve electrical stimulation system programmer
Programming Software
LIVANOVA USA, INC.
250 v10.0
In Commercial Distribution
- 05425025750382 ()
- Vagus nerve electrical stimulation system programmer
Programming Software
LIVANOVA USA, INC.
250 v11.0
In Commercial Distribution
- 05425025750375 ()
- Vagus nerve electrical stimulation system programmer
Programming Software
LIVANOVA USA, INC.
250 v11.0
In Commercial Distribution
- 05425025750368 ()
- Vagus nerve electrical stimulation system programmer
Programming Software
LIVANOVA USA, INC.
250 v10.0
In Commercial Distribution
- 05425025750214 ()
- Vagus nerve electrical stimulation system programmer
Programming Software
LIVANOVA USA, INC.
250 v8.1 (X5)
In Commercial Distribution
- 05425025750191 ()
- Vagus nerve electrical stimulation system programmer
Programming Software
LIVANOVA USA, INC.
250 v8.1 (X50)
In Commercial Distribution
- 05425025750184 ()
- Vagus nerve electrical stimulation system programmer
Programming Wand
LIVANOVA USA, INC.
2000
In Commercial Distribution
- 05425025750177 ()
- Vagus nerve electrical stimulation system programmer
Programming Wand
LIVANOVA USA, INC.
201
In Commercial Distribution
- 05425025750160 ()
- Vagus nerve electrical stimulation system programmer
Indications for Use:
CEFALY Connected is indicated to be used for:
Acute treatment of migraine with or without aura in patients 18 years of age or older.
Prophylactic treatment of migraine in patients 18 years of age or older.
Cefaly Technology SPRL
CEFALY Connected Bundle VA
In Commercial Distribution
- 05425018850334 ()
10811
- Craniofacial analgesia electrical stimulator
Hypoallergenic Electrode CEFALY Enhanced Kit (3 electrodes)
Cefaly Technology SPRL
11302
In Commercial Distribution
- 05425018850181 ()
- 05425018850310 ()
- Craniofacial analgesia electrical stimulator
CEFALY Enhanced Electrode Kit .3 electrodes
Cefaly Technology SPRL
11301
In Commercial Distribution
- 05425018850174 ()
- 05425018850303 ()
- Craniofacial analgesia electrical stimulator
CEFALY Connected is indicated to be used for:
Acute treatment of migraine with or without aura in patients 18 years of age or older.
Preventative treatment of migraine in patients 18 years of age or older.
Cefaly Technology SPRL
CEFALY Connected
In Commercial Distribution
- 05425018850297 ()
10801
- Craniofacial analgesia electrical stimulator
CEFALY Enhanced is for patients diagnosed by a physician with migraines per the FDA cleared indications for use.
CEFALY Enhanced is indicated to be used for:
Acute treatment of migraine with or without aura in patients 18 years of age or older.
Preventative treatment of migraine in patients 18 years of age or older.
Cefaly Technology SPRL
CEFALY Enhanced
In Commercial Distribution
- 05425018850280 ()
10701
- Craniofacial analgesia electrical stimulator
Cefaly DUAL Enhanced is a newer version of Cefaly DUAL which is an FDA - cleared device
Indications for Use:
CEFALY DUAL Enhanced is for patients diagnosed by a physician with migraines per the FDA cleared indications for use.
CEFALY DUAL Enhanced is indicated to be used for:
The acute treatment of migraine with or without aura in patients 18 years of age or older.
The preventative treatment of episodic migraine in patients 18 years of age or older.
Cefaly Technology SPRL
CEFALY DUAL Enhanced
In Commercial Distribution
- 05425018850273 ()
10601
- Craniofacial analgesia electrical stimulator
The Cefaly® Prevent device is indicated for the prophylactic treatment of episodic migraine in adults.
Cefaly Technology SPRL
Prevent
10230
- Craniofacial analgesia electrical stimulator
The Cefaly® Dual device is indicated for:
- The acute treatment of migraine with or without aura in patients 18 years of age or older.
- The prophylactic treatment of episodic migraine in patients 18 years of age or older.
Cefaly Technology SPRL
Dual
In Commercial Distribution
- 05425018850259 ()
10505
- Craniofacial analgesia electrical stimulator
The Cefaly® Acute device is indicated for the acute treatment of migraine with or without aura in patients 18 years of age or older.
Cefaly Technology SPRL
Acute
In Commercial Distribution
- 05425018850242 ()
10405
- Craniofacial analgesia electrical stimulator
Kit 3 Electrodes Blue Gel for Cefaly II
Cefaly Technology SPRL
11202
In Commercial Distribution
- 05425018850150 ()
- 05425018850181 ()
- Craniofacial analgesia electrical stimulator
Kit 3 electrodes for Cefaly II
Cefaly Technology SPRL
11201
In Commercial Distribution
- 05425018850143 ()
- 05425018850174 ()
- Craniofacial analgesia electrical stimulator
Set Cefaly® :
- Instruction manual
- Cefaly® device
- Cefaly® electrode
- Storage box
- Power adapter + cable
Cefaly Technology SPRL
10205
In Commercial Distribution
- 05425018850129 ()
- Craniofacial analgesia electrical stimulator
Kit 3 electrodes Blue Gel for Cefaly I
Cefaly Technology SPRL
11106
In Commercial Distribution
- 05425018850105 ()
- 05425018850204 ()
- Craniofacial analgesia electrical stimulator
Kit 3 electrodes for Cefaly I
Cefaly Technology SPRL
11101
In Commercial Distribution
- 05425018850044 ()
- 05425018850198 ()
- Craniofacial analgesia electrical stimulator
TRUMATCH Midface/Mandible - Titanium 3D Printed Implant for Orbit, Thin
Materialise NV
SD980.113
In Commercial Distribution
- 05420060381133 ()
SD980.113
- Custom-made cranial bone prosthesis
TRUMATCH Midface/Mandible - Titanium 3D Printed Orbital kit, without planning
Materialise NV
SD980.111
In Commercial Distribution
- 05420060381119 ()
SD980.111
- Craniofacial fixation plate kit, non-bioabsorbable
TRUMATCH Midface/Mandible - Titanium 3D Printed Orbital kit
Materialise NV
SD980.110
In Commercial Distribution
- 05420060381102 ()
- Craniofacial fixation plate kit, non-bioabsorbable
TRUMATCH TI Implant - Mandible - large
Materialise NV
SD980.109
In Commercial Distribution
- 05420060381096 ()
SD980.109
- Craniofacial fixation plate kit, non-bioabsorbable
TRUMATCH TI Implant - Mandible - medium
Materialise NV
SD980.108
In Commercial Distribution
- 05420060381089 ()
SD980.108
- Craniofacial fixation plate kit, non-bioabsorbable
TRUMATCH TI Implant - Mandible -small
Materialise NV
SD980.107
In Commercial Distribution
- 05420060381072 ()
SD980.107
- Craniofacial fixation plate kit, non-bioabsorbable
TRUMATCH TI Implant - Midface Small
Materialise NV
SD980.106
In Commercial Distribution
- 05420060381065 ()
SD980.106
- Craniofacial fixation plate kit, non-bioabsorbable