FDA UDI In Commercial Distribution 🇺🇸 United States

iFuse Implant System-Navigation – Impactor

DI: 00851085007633 · Model: 400194 · Si-Bone Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iFuse Implant System-Navigation – Impactor
Primary DI
00851085007633
Version / Model
400194
Company Name
Si-Bone Inc.
Labeler DUNS
830127168
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-29
Public Version
4
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
25246de0-9e09-4525-b5a0-5364eef7f1db

Device Description

Navigation, Impactor

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
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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
OLO Orthopedic Stereotaxic Instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00851085007633

Customer Contacts

Phone
855-884-3873