| Primary Device ID | 60889978024391 |
| NIH Device Record Key | 506bfd2a-ec5b-4eaa-9f5b-626f7296abd3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RVG 6100 |
| Version Model Number | RVG 6100 |
| Catalog Number | 8024390 |
| 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 | 60889978024391 [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 |
| 60889978024391 | RVG 6100 #2 Operatory Kit |
| 60889978024377 | RVG 6100 #0 Operatory Kit |
| 60889978024360 | 6100 Size 2 Upgrade |
| 60889978024353 | 6100 Size 1 Upgrade |
| 60889978001491 | 6100 SZ 0 Upgrade |
| 60889975314167 | RVG 6100 - SIZE 0 w/o USB HUB |
| 60889975314129 | RVG 6100 - SIZE 2 w/o USB HUB |
| 60889975314112 | RVG 6100 - SIZE 1 w/o USB HUB |
| 60889975155111 | RVG 6100 - SIZE 0 |
| 60889975154824 | RVG 6100 -SIZE 1 |
| 60889975154817 | RVG 6100 - SIZE 2 |
| 60889974007701 | CAPTEUR RVG 6100 T2 FLASH |
| 60889974007695 | CAPTEUR RVG 6100 T1 FLASH |
| 60889974007688 | CAPTEUR RVG 6100 T0 |