Primary Device ID | 50382903059244 |
NIH Device Record Key | 90512c3c-072c-497e-b4a8-4b0966c3b12f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Luer-Lok, BD SafetyGlide |
Version Model Number | 305924 |
Catalog Number | 305924 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 50 |
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 | 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 | 00382903059249 [Unit of Use] |
GS1 | 30382903059240 [Primary] |
GS1 | 50382903059244 [Package] Contains: 30382903059240 Package: Case [8 Units] In Commercial Distribution |
MEG | SYRINGE, ANTISTICK |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-09-12 |
Device Publish Date | 2016-09-16 |
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