| Primary Device ID | 60889971069405 |
| NIH Device Record Key | 26e84b63-867e-4e5a-878f-d6a63290904a |
| Commercial Distribution Discontinuation | 2017-12-12 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Vita Flex CR System |
| Version Model Number | Vita Flex CR System |
| Catalog Number | 1069400 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 60889971069405 [Primary] |
| MQB | Solid state x-ray imager (flat panel/digital imager) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2016-09-16 |
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| 60889971746320 | TRIMAX CR SYSTEM 40 MADE IN CH, PC/M |
| 60889971069443 | UPGRADE Vita Flex 30 to 45 PPH |
| 60889971069412 | NB Vita Flex CR 45PPH solution PC/Monito |
| 60889971069405 | NB Vita Flex CR 30PPH solution PC/Monito |
| 60889971069382 | Vita Flex CR 45PPH solution PC/Monitor |
| 60889971069375 | Vita Flex CR 30PPH solution PC/Monitor |
| 60889971069306 | Vita Flex CR System 45PPH |
| 60889971067241 | Vita Flex CR System 30PPH |
| 60889976579367 | VITA FLEX CR SYSTEM, NB 60PPH WITH PC&MO |
| 60889976579343 | VITA FLEX CR SYSTEM 60PPH WITH PC&MONITO |
| 60889976579336 | VITA FLEX CR SYSTEM 60PPH |