Primary Device ID | 00815212023484 |
NIH Device Record Key | 7c4b85e2-6d95-450a-a0c8-ad295d3b9935 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KIT:VCF TREATMENT,RIGHT,FRACTURE |
Version Model Number | KIV2100 |
Company DUNS | 933506164 |
Company Name | Izi Medical Products, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |