Primary Device ID | 00382902606697 |
NIH Device Record Key | 633c74cb-8f30-4c28-abd1-4a8725855f56 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD BBL™ Sensi-Disc™ 12-Place Dispenser Cannister |
Version Model Number | 260669 |
Catalog Number | 260669 |
Company DUNS | 122561087 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)638-8663 |
Technical_services@bd.com | |
Phone | +1(800)638-8663 |
Technical_services@bd.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382902606697 [Primary] |
JTN | SUSCEPTIBILITY TEST DISCS, ANTIMICROBIAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-05-19 |
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