| Primary Device ID | 00817330025401 |
| NIH Device Record Key | 49a66515-c53f-44f7-82d3-41e1f75e4e2c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | H.A.M., 03-Channel, 130cm cath, Varian-Gammamed |
| Version Model Number | 9102-GM-03 |
| Catalog Number | 9102-GM-03 |
| Company DUNS | 073260622 |
| Company Name | MICK RADIO NUCLEAR INSTRUMENT, INC |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 | 00817330025401 [Primary] |
| JAQ | System, Applicator, Radionuclide, Remote-Controlled |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00817330025401]
Moist Heat or Steam Sterilization
[00817330025401]
Moist Heat or Steam Sterilization
[00817330025401]
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 | 2016-09-22 |