Primary Device ID | B39057S000301 |
NIH Device Record Key | 4ea5b40e-f702-4e11-a080-1ff79d05696d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reprocessed Drill Bit, Sterilemica Cannulated, 3.0mm |
Version Model Number | 57S00030 |
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 |