Primary Device ID | 50382903032780 |
NIH Device Record Key | be63c267-33eb-4a64-9e1b-ab8822e4c36e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Eclipse Needle |
Version Model Number | 303278 |
Catalog Number | 303278 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
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 | 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 | 00382903032785 [Primary] |
GS1 | 50382903032780 [Package] Contains: 00382903032785 Package: Case [6000 Units] In Commercial Distribution |
FMI | Needle, hypodermic, single lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-21 |
Device Publish Date | 2024-11-13 |
00382903059041 - BD SafetyGlide | 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 25X5/8 RB |
00382903059058 - BD SafetyGlide | 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 23X1 RB |
00382903059065 - BD SafetyGlide | 2025-08-07 SYRINGE 3ML LL W/NDL SFTYGLD 22X1-1/2 RB |
00382903059096 - BD SafetyGlide | 2025-08-07 SYR 3ML LL W/NDL SFTYGLD 21X1-1/2 RB TW |
00382903059157 - BD SafetyGlide | 2025-08-07 NEEDLE SFTYGLD 21X1 RB TW |
00382903059164 - BD SafetyGlide | 2025-08-07 NEEDLE SFTYGLD 25X1 RB |
00382903059171 - BD SafetyGlide | 2025-08-07 NEEDLE SFTYGLD 21X1-1/2 RB TW |
00382903059188 - BD SafetyGlide | 2025-08-07 NEEDLE SFTYGLD 18X1-1/2 RB |