Primary Device ID | 10841307118848 |
NIH Device Record Key | 31812e9f-f294-45ab-a84f-771ff530b886 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IMZ 3.3mm Diameter Ti IMC Conversion Abutment |
Version Model Number | 57-8318CU |
Catalog Number | 57-8318CU |
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 | 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 |