Primary Device ID | 00840682113205 |
NIH Device Record Key | d963e1eb-3a1a-4980-b926-d9cc418a5e23 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 7S |
Company DUNS | 623906971 |
Company Name | GE PARALLEL DESIGN, 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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |
Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682113205 [Primary] |
IYN | System, imaging, pulsed doppler, ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-01-17 |
Device Publish Date | 2016-07-15 |
00840682142366 - NA | 2020-08-17 |
00840682108676 - NA | 2020-05-05 |
00840682113045 - NA | 2019-01-21 |
00840682105231 - NA | 2019-01-18 |
00840682105248 - NA | 2019-01-18 |
00840682105255 - NA | 2019-01-18 |
00840682115216 - NA | 2019-01-18 |
00840682105262 - NA | 2019-01-17 |