NormaTec Pulse Pro 10200

GUDID 00817369020019

Sequential venous compression system Sequential venous compression system Sequential venous compression system

Primary Device ID	00817369020019
NIH Device Record Key	d0898526-3277-4d6d-981f-794ab76aebe3
Commercial Distribution Status	In Commercial Distribution
Brand Name	NormaTec Pulse Pro
Version Model Number	JMS4T
Catalog Number	10200
Company DUNS	111448069
Company Name	NORMATEC INDUSTRIES LP
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Storage Environment Atmospheric Pressure	Between 19 KiloPascal and 106 KiloPascal
Storage Environment Atmospheric Pressure	Between 19 KiloPascal and 106 KiloPascal
Storage Environment Atmospheric Pressure	Between 19 KiloPascal and 106 KiloPascal

Device Issuing Agency	Device ID
GS1	00817369020019 [Primary]

IRP	Massager, Powered Inflatable Tube

Steralize Prior To Use	false
Device Is Sterile	false