Primary Device ID | 00888118095688 |
NIH Device Record Key | 5349c4a0-cb9c-4a88-8e6b-e365eb188251 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LEVEL ONE, STERILE |
Version Model Number | 25-043-95-71 |
Company DUNS | 826499238 |
Company Name | KLS-Martin L.P. |
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 |