Primary Device ID | 50885403422339 |
NIH Device Record Key | ed407817-6f6c-4405-8931-804d9d34aa5d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedSystem III |
Version Model Number | 28006 |
Catalog Number | 28006 |
Company DUNS | 360624720 |
Company Name | CAREFUSION 303, INC. |
Device Count | 20 |
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 | false |
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 | 10885403422331 [Unit of Use] |
GS1 | 50885403422339 [Primary] |
LZH | PUMP, INFUSION, ENTERAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-20 |
Device Publish Date | 2017-07-27 |
50885403422377 | MSIII LGT SNSTV SET |
50885403422360 | MedSystem III Infusion Set |
50885403422353 | MSIII BURETTE 60 DROP W/.2 FIL |
50885403422346 | MedSystem III Infusion Half Set |
50885403422339 | ENTERAL SET W/O BAG MSIII(BOM) |
50885403274990 | MedSystem III Infusion Blood Set |
50885403274976 | MedSystem III Low Sorbing Infusion Set |
50885403274969 | MedSystem III Infusion Set |
50885403274945 | MedSystem III Infusion Set |
50885403274938 | MedSystem III Infusion Set |
50885403274884 | MedSystem III Half Set |
50885403274846 | MedSystem III Infusion Set |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEDSYSTEM III 74610721 1952843 Live/Registered |
CAREFUSION 303, INC 1994-12-13 |
MEDSYSTEM III 74437536 not registered Dead/Abandoned |
IVAC Corporation 1993-09-20 |