Primary Device ID | 60889978024384 |
NIH Device Record Key | 8db80b24-8cbf-4263-ad9e-ba30ca36c0f1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RVG 6200 |
Version Model Number | RVG 6200 |
Catalog Number | 8024382 |
Company DUNS | 793169512 |
Company Name | CARESTREAM HEALTH, 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 | 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 |
Storage Environment Temperature | Between 10 Degrees Celsius and 24 Degrees Celsius |
Storage Environment Temperature | Between 10 Degrees Celsius and 24 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 60889978024384 [Primary] |
EAP | UNIT, X-RAY, INTRAORAL |
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 | 2016-09-16 |
60889978024384 | RVG 6100 #1 Operatory Kit |
60889975313993 | RVG 6200 #2 FOR USE W. RVG CONNECT |
60889975313986 | RVG 6200 #1 FOR USE W. RVG CONNECT |
60889975310725 | RVG 6200 SIZE 2 |
60889975310718 | RVG 6200 SIZE 1 |
60889974007503 | CAPTEUR RVG 6200 T2 |
60889974007459 | CAPTEUR RVG 6200 T1 |