| Primary Device ID | 60192155310720 |
| NIH Device Record Key | 556121b9-f114-4b1b-a107-7a38b516dcae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RVG 6200 |
| Version Model Number | RVG 6200 |
| Catalog Number | 5310727 |
| Company DUNS | 019796106 |
| Company Name | CARESTREAM DENTAL LLC |
| 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 | 60192155310720 [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 | 6 |
| Public Version Date | 2020-02-10 |
| Device Publish Date | 2018-01-15 |
| 60192155319488 | RVG 6200 #2 WITH RVG CONNECT FOR US |
| 60192155319464 | RVG 6200 #1 WITH RVG CONNECT FOR US |
| 60192155313998 | RVG 6200 #2 FOR USE W. RVG CONNECT |
| 60192155313981 | RVG 6200 #1 FOR USE W. RVG CONNECT |
| 60192155310720 | RVG 6200 SIZE 2 |
| 60192155310713 | RVG 6200 SIZE 1 |
| 60192155008085 | CAPTEUR RVG 6200 T2 CSD |
| 60192155008078 | CAPTEUR RVG 6200 T1 CSD |