Puregraft 850/PURE

GUDID 10860407002222

Autologous adipose tissue collection/washing set

Primary Device ID	10860407002222
NIH Device Record Key	b7eab9a2-60a4-4fc7-b3a6-6463929a56a1
Commercial Distribution Status	In Commercial Distribution
Brand Name	Puregraft
Version Model Number	850
Catalog Number	850/PURE
Company DUNS	079508934
Company Name	PUREGRAFT LLC
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	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00860407002225 [Primary]
GS1	10860407002222 [Package] Contains: 00860407002225 Package: Case [5 Units] In Commercial Distribution

MUU	System, Suction, Lipoplasty

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
PUREGRAFT 87760609 5554305 Live/Registered	PUREGRAFT LLC 2018-01-18
PUREGRAFT 77905359 3945551 Dead/Cancelled	PUREGRAFT LLC 2010-01-05