| Primary Device ID | 20020221269615 |
| NIH Device Record Key | f4bb8ebc-d6c4-4f7a-bb03-8cdb0583fdb3 |
| Commercial Distribution Discontinuation | 2023-04-21 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | EXEL Spinal Needle |
| Version Model Number | 26961 |
| Catalog Number | 26961 |
| Company DUNS | 180572216 |
| Company Name | Exel International |
| Device Count | 50 |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00020221269611 [Unit of Use] |
| GS1 | 10020221269618 [Primary] |
| GS1 | 20020221269615 [Package] Contains: 10020221269618 Package: [2 Units] Discontinued: 2023-04-21 Not in Commercial Distribution |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2023-04-24 |
| Device Publish Date | 2016-09-23 |
| 20020221269653 | Spinal Needle, 22G x 2 3/4, QUINCKE BEVEL |
| 20020221269707 | Spinal Needle, 25G x 3 1/2, QUINCKE BEVEL |
| 20020221269677 | Spinal Needle, 22G x 3 1/2, QUINCKE BEVEL |
| 20020221269646 | Spinal Needle, 20G x 3 1/2, QUINCKE BEVEL |
| 10020221269601 | Spinal Needle, 18G x 3 1/2, QUINCKE BEVEL |
| 20020221269615 | Spinal Needle, 20G x 2-3/4, QUINCKE BEVEL |