Primary Device ID | 18257200140114 |
NIH Device Record Key | a70cae75-1e71-4301-baaa-8bd7103d927e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Firebird SI Fusion |
Version Model Number | 18-1040SP |
Company DUNS | 927083808 |
Company Name | Orthofix US LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com | |
Phone | +1(800)527-0404 |
customerservice@orthofix.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 18257200140114 [Primary] |
OUR | Sacroiliac Joint Fixation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-20 |
Device Publish Date | 2024-12-12 |
18257200140114 | 11MM X 40MM FIREBIRD SI SCREW, FIREBIRD SI FUSION SYSTEM, STERILE |
18257200140107 | 11MM X 35MM FIREBIRD SI SCREW, FIREBIRD SI FUSION SYSTEM, STERILE |