Primary Device ID | 00815137020384 |
NIH Device Record Key | ab590b3f-dfd6-44a4-9def-54428c15e058 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | A-SPOT |
Version Model Number | 651 |
Company DUNS | 001157841 |
Company Name | Beekley Corporation |
Device Count | 120 |
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 | 00815137020384 [Primary] |
GS1 | 10815137020381 [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 |
00815137021770 | Palpable Mass Markers, uniform low-density see-through triangle |
00815137020384 | Palpable Mass Markers, uniform low-density see-through triangle |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
A-SPOT 86346096 4695701 Live/Registered |
Beekley Corporation 2014-07-23 |