FDA UDI In Commercial Distribution 🇺🇸 United States

Amplifine

DI: 00350224000134 · Model: 30ml - BD · SUNEVA MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Amplifine
Primary DI
00350224000134
Version / Model
30ml - BD
Catalog Number
SM-PRP-30-BD
Company Name
SUNEVA MEDICAL, INC.
Labeler DUNS
012844615
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-31
Public Version
2
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
7caa072a-ec12-468c-8dfe-52c15a6c9d3e

Device Description

Amplifine HD PRP Tube 30ml, Blood Draw kit

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
61377 Autologous platelet-based product centrifuge tube

Identifiers

Type ID
Primary 00350224000134

Customer Contacts

Phone
858-550-9999

Device Sizes

Type Value Unit Text
Total Volume 30 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 40 Degrees Celsius