FDA UDI Not in Commercial Distribution 🇺🇸 United States

Sonoma Orthopedic Products, Inc

DI: 00816988011989 · Model: Fibula Nail Procedure Pack · ARTHREX, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sonoma Orthopedic Products, Inc
Primary DI
00816988011989
Version / Model
Fibula Nail Procedure Pack
Catalog Number
ST6100
Company Name
ARTHREX, INC.
Labeler DUNS
131747628
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-19
Public Version
3
Public Version Date
2020-07-08
Public Version Status
Update
Public Device Record Key
b7b31493-ee8d-4dea-a7f7-38383ffa06ee
Distribution End Date
2020-07-07

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
Yes
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
HTW Bit, Drill
HTO Reamer
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00816988011989