Primary Device ID | 00840682114639 |
NIH Device Record Key | a37e92ce-5f55-4755-bcec-309ca84ce9ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DURA-CUF |
Version Model Number | 2750 |
Company DUNS | 784985108 |
Company Name | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)558-5120 |
xx@xx.xx |
Device Size Text, specify | 0 |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682110174 [Primary] |
GS1 | 00840682114639 [Package] Contains: 00840682110174 Package: [5 Units] In Commercial Distribution |
DXQ | blood pressure cuff |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2016-06-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DURA-CUF 73452293 1304884 Live/Registered |
Johnson & Johnson 1983-11-09 |