Vita Flex CR System 1069384

GUDID 60889971069382

Vita Flex CR 45PPH solution PC/Monitor

CARESTREAM HEALTH, INC.

Computed radiography digital imaging scanner Computed radiography digital imaging scanner

• Primary Device ID: 60889971069382
• NIH Device Record Key: 87c302e7-ba16-43a7-bf09-ef686c9d5f78
• 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: 1069384
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	60889971069382 [Primary]

FDA Product Code

• MQB: Solid state x-ray imager (flat panel/digital imager)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• 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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• 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