FDA UDI In Commercial Distribution 🇺🇸 United States

SFS

DI: 18257200057580 · Model: 59-1091 · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SFS
Primary DI
18257200057580
Version / Model
59-1091
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-19
Public Version
2
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
dfab182e-2f07-4e96-8534-38df2799a4cb

Device Description

SFS REDUCTION SCREW CADDY

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
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 18257200057580

Customer Contacts