Primary Device ID | 10841307114000 |
NIH Device Record Key | 772a3524-f1d6-44be-9217-e2de299d9b57 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Titanium Non-Engaging Temporary Abutment |
Version Model Number | 6050-49 |
Catalog Number | 6050-49 |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
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 | true |
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 |