FDA UDI In Commercial Distribution 🇺🇸 United States

Arthrex®

DI: 10888867121116 · Model: AR-7277 · ARTHREX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Arthrex®
Primary DI
10888867121116
Version / Model
AR-7277
Catalog Number
AR-7277
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2017-02-15
Public Version
6
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
1c8a840b-ce85-4afb-9f7c-3e36f0549f43

Device Description

SAILTAPE, 3.5MMX15MM, WHITE

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
Labeling does not contain MRI Safety Information
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
Primary 10888867121116
Unit of Use 00888867121119
Secondary M150AR72771

Customer Contacts