FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867084063 · Model: ABS-10100 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867084063
Version / Model
ABS-10100
Catalog Number
ABS-10100
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-15
Public Version
5
Public Version Date
2020-12-15
Public Version Status
Update
Public Device Record Key
aae95e13-0e32-47ae-a65a-51502c984807

Device Description

CART, ACP

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
Yes
PM Exempt
Yes
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
No

Product Codes

Code Name
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
40596 Electromechanical device/system transport trolley

Identifiers

Type ID
Primary 00888867084063

Customer Contacts