Primary Device ID | B390KM35241 |
NIH Device Record Key | a399fe85-5e60-43bf-9f83-3a630032eb43 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reprocessed Oscillating Sagittal Saw Blade, Thin, 25 x 5.5 x 0.38mm |
Version Model Number | KM3-524 |
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 |