FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 00888867315198 · Model: AR-1676TS · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Arthrex®
Primary DI
00888867315198
Version / Model
AR-1676TS
Catalog Number
AR-1676TS
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-06
Public Version
3
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
bab4a2ed-799c-44c1-ad59-37dab0c8ce9c

Device Description

Tenodesis Graft Sizing Kit

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
No
MRI Safety
MR Safe
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
GAT SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Package 10888867315195
Primary 00888867315198

Customer Contacts