Primary Device ID | 20020221269707 |
NIH Device Record Key | 67cbd0bc-eddd-42f9-80b1-50b85b047ac6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXEL Spinal Needle |
Version Model Number | 26970 |
Catalog Number | 26970 |
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 | 00020221269703 [Unit of Use] |
GS1 | 10020221269700 [Primary] |
GS1 | 20020221269707 [Package] Contains: 10020221269700 Package: [2 Units] In Commercial Distribution |
GS1 | 30020221269704 [Package] Package: Shipping carton [4 Units] In Commercial Distribution |
GS1 | 40020221269701 [Package] Contains: 10020221269700 Package: Shipping carton [10 Units] 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 | 2023-04-20 |
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 |