Primary Device ID | 08800023152210 |
NIH Device Record Key | 44bebbd9-f0cd-462b-8307-773941015eb5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REBORN Fixture |
Version Model Number | IC1R4513OC |
Company DUNS | 688248447 |
Company Name | Cybermed Inc. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |