Adstation Oto+
Diagnostix™ - 5681L-7
Device Description
A device designed to measure blood pressure consisting of an inflatable cuff that fits around a limb (arm or thigh), an inflation bulb for controlling the air pressure within the cuff, an aneroid manometer, and tubing. The aneroid manometer consists of a metal bellows, which expands as the pressure in the cuff increases, and a mechanical amplifier that transmits this expansion through a lever to an indicator needle, which rotates around a circular, calibrated scale. The manometer may be mounted to a wall, placed on a table, or hand held (portable); blood pressure measurement is taken in conjunction with a stethoscope.
Environmental Conditions
- 95.00
- 10.00
- 131.00
- 14.00
Device Sizes
No Data Available
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: DXQ
Device Name: Blood Pressure Cuff
Device Class: 2
Physical State: N/A
Definition: A blood pressure cuff is a device that has an inflatable bladder in an elastic sleeve (cuff) with a mechanism for inflating the bladder. The cuff is used to determine a subject's blood pressure.
Submission Type ID: 1
Review Panel: CV
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 870.1120
Third Party Flag: Y
Medical Specialty: CV
Code: HLJ
Device Name: Ophthalmoscope, Battery-Powered
Device Class: 2
Physical State: N/A
Definition: N/A
Submission Type ID: 4
Review Panel: OP
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 886.1570
Third Party Flag: N
Medical Specialty: OP
Code: ERA
Device Name: Otoscope
Device Class: 1
Physical State: N/A
Definition: N/A
Submission Type ID: 4
Review Panel: EN
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 874.4770
Third Party Flag: N
Medical Specialty: EN
Device IdentifiersDevice Id: 00634782093020
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A