FDA UDI In Commercial Distribution 🇺🇸 United States

Puregraft 50 System

DI: 00850034511696 · Model: 50/PURE · Bimini Technologies LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Puregraft 50 System
Primary DI
00850034511696
Version / Model
50/PURE
Company Name
Bimini Technologies LLC
Labeler DUNS
076649467
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-11
Public Version
1
Public Version Date
2024-01-19
Public Version Status
New
Public Device Record Key
53d636d5-fead-4476-84d4-e9cf9f09bb6f

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
QKL Lipoaspirate Washing System For Aesthetic Body Contouring

GMDN Terms

Code Name
56627 Autologous adipose tissue collection/washing set

Identifiers

Type ID
Package 00850034511719
Primary 00850034511696