FDA UDI In Commercial Distribution 🇺🇸 United States

Amplifine

DI: 00850034511290 · Model: AMPLIFINE · Bimini Technologies LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Amplifine
Primary DI
00850034511290
Version / Model
AMPLIFINE
Company Name
Bimini Technologies LLC
Labeler DUNS
076649467
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-09
Public Version
1
Public Version Date
2022-02-17
Public Version Status
New
Public Device Record Key
799ecd62-cd05-4826-8d6d-56a5674dc5ee

Device Description

A sterile, single use, syringe assembly that is intended for separating and concentrating blood components along with the use of a desktop centrifuge. It enables blood to be separated and aspirated in a single device after they have been centrifuged.

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
ORG Platelet And Plasma Separator For Bone Graft Handling

GMDN Terms

Code Name
46923 Haematological concentrate system preparation kit, platelet concentration

Identifiers

Type ID
Package 00850034511887
Primary 00850034511290

Premarket Submissions

Submission Number Supplement Number
BK200449 0