Primary Device ID | 15420045514638 |
NIH Device Record Key | e64722af-b7d6-4ec4-90a5-87babce249a7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TruNode |
Version Model Number | 120-807611 |
Catalog Number | 120-807611 |
Company DUNS | 018925968 |
Company Name | Hologic, Inc. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 | 15420045514638 [Primary] |
IZD | Probe, uptake, nuclear |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-25 |
Device Publish Date | 2022-04-16 |
15420045514416 | 120-807606 |
15420045514638 | 120-807611 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRUNODE 86519309 4838402 Live/Registered |
FAXITRON BIOPTICS, LLC 2015-01-30 |