FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867319950 · Model: ABS-2016-03 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867319950
Version / Model
ABS-2016-03
Catalog Number
ABS-2016-03
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-20
Public Version
5
Public Version Date
2021-09-21
Public Version Status
Update
Public Device Record Key
865040ce-b0dc-41e4-828f-28c1444a89a0

Device Description

BioSurge III with 15x40x3mm DBM Strips

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
Yes
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
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
Primary 00888867319950

Customer Contacts