Primary Device ID | B390KM34141 |
NIH Device Record Key | a008db81-407e-44e6-82a5-c29cb50f1ad2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reprocessed Small Bone Osc Sagittal Blade, 25 x 5.5 x 0.38mm |
Version Model Number | KM3-414 |
Company DUNS | 785616934 |
Company Name | SURETEK MEDICAL |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |