FDA UDI In Commercial Distribution 🇺🇸 United States

Puregraft 850 System

DI: 00850034511191 · Model: 850/PURE · Bimini Technologies LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Puregraft 850 System
Primary DI
00850034511191
Version / Model
850/PURE
Company Name
Bimini Technologies LLC
Labeler DUNS
076649467
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-01
Public Version
1
Public Version Date
2022-04-11
Public Version Status
New
Public Device Record Key
b8b3a05a-bd3b-4fa9-a7d1-513f4a471744

Device Description

A sterile, single use, closed polyolefin bag contains two polyester meshes and breached by valves for use in harvesting, filtering, and transferring autologous fat tissue for reinjecting back into the same patient.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MUU System, Suction, Lipoplasty

GMDN Terms

Code Name
56627 Autologous adipose tissue collection/washing set

Identifiers

Type ID
Package 00850034511207
Primary 00850034511191

Premarket Submissions

Submission Number Supplement Number
K113255 000