FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867083974 · Model: ABS-10060 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867083974
Version / Model
ABS-10060
Catalog Number
ABS-10060
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
7
Public Version Date
2022-12-16
Public Version Status
Update
Public Device Record Key
0135483c-66f8-4ec7-8a9c-f67a9315b9e7

Device Description

ANGEL PRP SYSTEM CENTRIFUGE US (NEW)

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

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 00888867083974
Secondary M150ABS100600

Customer Contacts