FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867084001 · Model: ABS-10063 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867084001
Version / Model
ABS-10063
Catalog Number
ABS-10063
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-15
Public Version
3
Public Version Date
2020-01-28
Public Version Status
Update
Public Device Record Key
77865975-949a-4d05-90a1-c5980d08eb3b

Device Description

ANGEL cPRP PROCESSING SET US

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
60336 Blood centrifugation system

Identifiers

Type ID
Primary 00888867084001
Secondary M150ABS100630
Package 10888867084008

Customer Contacts