SEARCH RESULTS FOR: !➧주식DB구합니다◀✅텔레그램thinkDB(13636 results)

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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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Tenex Health TX® - 00857156006147

TX2 MicroTip
TENEX HEALTH, INC.
554-2002-001
In Commercial Distribution

  • 00857156006147 ()


  • Ultrasonic suction system

Tenex Health TX® - 00857156006093

TX-Bone (TXB) Procedure Pack
TENEX HEALTH, INC.
554-3003-001
In Commercial Distribution

  • 00857156006109 ()
  • 00857156006093 ()
  • 00857156006116 ()
554-3003-001

  • Ultrasonic suction system

Tenex Health TX® - 00857156006086

TX Supply Kit
TENEX HEALTH, INC.
554-1001-001
In Commercial Distribution

  • 00857156006086 ()


  • Ultrasonic suction system

Tenex Health TX® - 00857156006079

TX-Bone (TXB) MicroTip
TENEX HEALTH, INC.
557-1002-001
In Commercial Distribution

  • 00857156006079 ()


  • Ultrasonic suction system

PulStar - 00855341008006

The PulStar Spine Mobilization Device is intended for use by chiropractors, physical therapists and physicians for mobilization of the spine. The device consists of a hand-held impulse head attached to an electronic control module. The control module is connected to an Apple computer through a USB cable. Appropriate software is used to display the results of tissue compliance measurements. Intended Use and operation: Intended use of the PulStar is for the treatment of musculoskeletal pain due to joint subluxation, restricted joint mobility, myofacial spasm and ligamentous strain. The clinician uses a hand held impulse head to test the stiffness of the patient’s spine at each vertebral level, the results of this procedure are recorded in the patient file in a computer database and displayed on the computer screen. The clinician then decides where therapy is needed and applies multiple impulses with the impulse head to those areas of the body of the patient with the intent of reducing spinal stiffness. After treatment, the clinician repeats the initial test of the patient’s spine to document changes in stiffness effected by the therapy.
Sense Technology, Inc.
G3
In Commercial Distribution

  • 10855341008003 ()
  • 00855341008006 ()


  • Joint/spinal manipulator, electronic

Dukal - 00665973017778

Oil Emulsion Dressing 5" x 9"
Dukal LLC
224
In Commercial Distribution

  • 10665973017775 ()
  • 00665973017778 ()
  • 20665973017772 ()
224

  • Petrolatum woven gauze pad

Dukal - 00665973017259

Plain Packing Strip 1/4" x 5 yd
Dukal LLC
260
In Commercial Distribution

  • 00665973017259 ()
  • 20665973017253 ()
  • 10665973017256 ()
260

  • Gauze strip, non-antimicrobial

Dukal - 00665973017242

Plain Packing Strip 1/2" x 5 yd
Dukal LLC
261
In Commercial Distribution

  • 10665973017249 ()
  • 00665973017242 ()
  • 20665973017246 ()
261

  • Gauze strip, non-antimicrobial

Dukal - 00665973017235

Plain Packing Strip 1" x 5 yd
Dukal LLC
262
In Commercial Distribution

  • 10665973017232 ()
  • 00665973017235 ()
  • 20665973017239 ()
262

  • Gauze strip, non-antimicrobial

Dukal - 00665973017228

Plain Packing Strip 2" x 5yd
Dukal LLC
263
In Commercial Distribution

  • 10665973017225 ()
  • 00665973017228 ()
  • 20665973017222 ()
263

  • Gauze strip, non-antimicrobial
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