Primary Device ID | 00816131021872 |
NIH Device Record Key | 5136c079-a247-4ca1-8afe-37fab7019f7d |
Commercial Distribution Discontinuation | 2016-12-29 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Rodo Abutment |
Version Model Number | 53025NBA221 |
Catalog Number | 53025NBA221 |
Company DUNS | 004584361 |
Company Name | RODO MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
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 | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |