FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867057708 · Model: AR-9144-19P · ARTHREX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867057708
Version / Model
AR-9144-19P
Catalog Number
AR-9144-19P
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
4
Public Version Date
2019-10-17
Public Version Status
Update
Public Device Record Key
44cfc6f4-407b-4251-a936-0453d43b7b29

Device Description

USP II HUMERAL HEAD 44/19

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
No
MRI Safety
MR Conditional
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
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED

GMDN Terms

Code Name
35670 Total shoulder prosthesis

Identifiers

Type ID
Primary 00888867057708
Secondary M150AR914419P1

Customer Contacts