RENPHO Air Compression Therapy Device

GUDID 10810140061239

Multi-chamber venous compression system garment, reusable

Primary Device ID	10810140061239
NIH Device Record Key	b5a03c76-2517-4272-bbfa-3c61d500898e
Commercial Distribution Status	In Commercial Distribution
Brand Name	RENPHO Air Compression Therapy Device
Version Model Number	RP-ALM076H
Company DUNS	033774836
Company Name	Joicom Corporation
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	false

Device Issuing Agency	Device ID
GS1	00810140061232 [Primary]
GS1	10810140061239 [Package] Contains: 00810140061232 Package: [6 Units] In Commercial Distribution

IRP	Massager, Powered Inflatable Tube

Steralize Prior To Use	false
Device Is Sterile	false