Primary Device ID | 60192155313998 |
NIH Device Record Key | 49f47081-6e73-453a-853c-be56f46ad1ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RVG 6200 |
Version Model Number | RVG 6200 |
Catalog Number | 5313994 |
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 | 60192155313998 [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 |