Primary Device ID | 00860009184503 |
NIH Device Record Key | bd9ab582-3372-4f8e-a772-7ff0ee63468f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BeamSite |
Version Model Number | BeamSite |
Company DUNS | 079605332 |
Company Name | Doseoptics 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 | false |
Lot Batch | true |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860009184503 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-18 |
Device Publish Date | 2023-08-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BEAMSITE 97163877 not registered Live/Pending |
DoseOptics LLC 2021-12-09 |