Primary Device ID | 05206569560046 |
NIH Device Record Key | 0dc71934-f834-4683-be01-8a89efd35198 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BONASIL A+ Putty |
Version Model Number | Fast Set, 400g Base + 400g Catalyst |
Catalog Number | 210101800F |
Company DUNS | 728534814 |
Company Name | DMP DENTAL INDUSTRY S.A. |
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 | false |
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 |