| Primary Device ID | 00817330021908 |
| NIH Device Record Key | bd47cf9d-20ff-4cfd-a103-f33aa81514fb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CT/MR R&T IU Tube, 30ø,4.0cm, Nucletron |
| Version Model Number | 0820-30-4 |
| Catalog Number | 0820-30-4 |
| Company DUNS | 073260622 |
| Company Name | MICK RADIO NUCLEAR INSTRUMENT, INC |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817330021908 [Primary] |
| JAQ | System, Applicator, Radionuclide, Remote-Controlled |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00817330021908]
Moist Heat or Steam Sterilization
[00817330021908]
Moist Heat or Steam Sterilization
[00817330021908]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-26 |