DriSate DF-120

GUDID 00814963020582

Haemodialysis concentrate

Primary Device ID	00814963020582
NIH Device Record Key	d74e96d5-cc22-4660-aa18-9b8324c5bbdb
Commercial Distribution Status	In Commercial Distribution
Brand Name	DriSate
Version Model Number	DF-120
Catalog Number	DF-120
Company DUNS	933721433
Company Name	ROCKWELL MEDICAL, INC.
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
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	00814963020582 [Primary]

KPO	Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

Steralize Prior To Use	false
Device Is Sterile	false