| Primary Device ID | 00840996163712 |
| NIH Device Record Key | 5604d740-5c95-4767-820a-42dfef1e221c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Octane Straight IR |
| Version Model Number | PT23-36116 |
| Company DUNS | 078293017 |
| Company Name | Choice Spine, LP |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| Manufacturing Date | false |
| 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 |
| Phone | +1(865)246-3333 |
| info@choicespine.net |
| Length | 10 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840996163712 [Primary] |
| MPQ | CONTAINER, SPECIMEN, URINE, DRUGS OF ABUSE, OVER THE COUNTER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00840996163712]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2017-09-20 |
| 00840996163804 | OCTANE STRAIGHT IR, Ti, 32X10X15, 6 DEG |
| 00840996163798 | OCTANE STRAIGHT IR, Ti, 32X10X14, 6 DEG |
| 00840996163781 | OCTANE STRAIGHT IR, Ti, 32X10X13, 6 DEG |
| 00840996163774 | OCTANE STRAIGHT IR, Ti, 32X10X12, 6 DEG |
| 00840996163767 | OCTANE STRAIGHT IR, Ti, 32X10X11, 6 DEG |
| 00840996163750 | OCTANE STRAIGHT IR, Ti, 36X10X15, 6 DEG |
| 00840996163743 | OCTANE STRAIGHT IR, Ti, 36X10X14, 6 DEG |
| 00840996163736 | OCTANE STRAIGHT IR, Ti, 36X10X13, 6 DEG |
| 00840996163729 | OCTANE STRAIGHT IR, Ti, 36X10X12, 6 DEG |
| 00840996163712 | OCTANE STRAIGHT IR, Ti, 36X10X11, 6 DEG |