Home GUDID 00844064035550
Spectrum
Primary DI 00844064035550
Brand Spectrum
Company RADIA ENTERPRISES, INC.
Model SM109
Device description Aneroid Sphygmomanometer
Published 2019-05-10
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC true
Sterile false
Single use false
Product Codes# Code, Name table Code Name DXN System, Measurement, Blood-Pressure, Non-Invasive
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00844064035550 Package GS1 50 In Commercial Distribution 00844064035567 Package GS1 1 In Commercial Distribution 00844064049335 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00844064035550 00844064035550 844064035550 0844064035550 00844064035567 00844064035567 844064035567 0844064035567 00844064049335 00844064049335 844064049335 0844064049335
GMDN Terms# Term, Definition table Term Definition Aneroid manual sphygmomanometer 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.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature -20 Degrees Celsius 70 Degrees Celsius
Regulatory Flags# DUNS number 039675442 Device count 1 DM exempt true Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label false Donation ID number false Contains natural rubber latex true No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00844064049335 Spectrum SM109 2019-05-10 00844064035635 Spectrum SM109 2017-03-07
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