Primary Device ID | 50382903686082 |
NIH Device Record Key | 5451bd8e-7edc-4628-9b05-d84080768fa5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Becton Dickinson and Company, USA 22G x 1 1/4 |
Version Model Number | 368608 |
Catalog Number | 368608 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 480 |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382903686087 [Unit of Use] |
GS1 | 50382903686082 [Primary] |
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 | 4 |
Public Version Date | 2019-01-08 |
Device Publish Date | 2016-07-28 |
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