Primary Device ID | 00815137020186 |
NIH Device Record Key | 3c3d29f2-b60b-4753-8b96-ba3f77e2fe98 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Localizers |
Version Model Number | 210 |
Company DUNS | 001157841 |
Company Name | Beekley Corporation |
Device Count | 40 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815137020186 [Primary] |
GS1 | 10815137020183 [Unit of Use] |
JAC | System, X-Ray, Film Marking, Radiographic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-30 |
Device Publish Date | 2019-07-22 |
00815137021534 | Diagnostic CT Skin Markers, 4.0mm low-density pellet |
00815137021527 | Diagnostic CT Skin Markers, 2.3mm low-density pellet |
00815137021091 | Diagnostic CT Skin Markers, 4.0mm low-density pellet |
00815137020186 | Diagnostic CT Skin Markers, 2.3mm low-density pellet |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LOCALIZERS 77264841 not registered Dead/Abandoned |
Localizers LLC 2007-08-27 |