Primary Device ID | 00840682107723 |
NIH Device Record Key | a9dd5489-9d1d-4cc6-bf81-70f7cb0bddd0 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | RAB4-8L |
Company DUNS | 300599979 |
Company Name | GE Healthcare Austria GmbH & Co OG |
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 Atmospheric Pressure | Between 70 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682107723 [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 | 2018-07-06 |
Device Publish Date | 2016-07-15 |
00195278677587 - Voluson | 2023-11-23 Voluson Exp to BT24 UPG |
00195278699848 - Voluson | 2023-11-23 Voluson Expert 22 BT24 |
00195278699800 - Voluson | 2023-11-15 Voluson Expert 18 BT24 |
00195278699824 - Voluson | 2023-11-15 Voluson Expert 20 BT24 |
00195278283375 - RIC10-D | 2023-10-19 RIC10-D |
00195278347473 - Voluson | 2022-08-24 Voluson Expert 18 |
00195278347480 - Voluson | 2022-08-24 Voluson Expert 20 |
00195278347497 - Voluson | 2022-06-22 Voluson Expert 22 |