Primary Device ID | 00812444023053 |
NIH Device Record Key | 3ebfae75-8e5d-49df-9272-803487149c6b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GOLD FIDUCIAL MARKER |
Version Model Number | RT4423K-18-5-1 |
Company DUNS | 964053560 |
Company Name | RIVERPOINT MEDICAL, 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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812444023053 [Primary] |
KXK | Source, Brachytherapy, Radionuclide |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00812444023091 | BRACHYTHERAPY |
00812444023084 | BRACHYTHERAPY |
00812444023077 | BRACHYTHERAPY |
00812444023060 | BRACHYTHERAPHY |
00812444023053 | BRACHYTHERAPY |
00812444023046 | BRACHYTHERAPY |
00812444023039 | BRACHYTHERAPY |
00812444023022 | BRACHYTHERAPY |
00812444023015 | BRACHYTHERAPY |
00812444023008 | BRACHYTHERAPY |
00812444022995 | BRACHYTHERAPHY |
00812444022988 | BRACHYTHERAPY |
00812444022971 | BRACHYTHERAPY |