MIN-R EV 150 Screen 8838336

GUDID 60889978838332

SGL 18X24CM MINR EV150 S WO FM FOEM

CARESTREAM HEALTH, INC.

X-ray intensifying screen X-ray intensifying screen

• Primary Device ID: 60889978838332
• NIH Device Record Key: ad6da5d7-3543-4e0e-932c-78795703fb35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MIN-R EV 150 Screen
• Version Model Number: MIN-R EV 150 Screen
• Catalog Number: 8838336
• Company DUNS: 793169512
• Company Name: CARESTREAM HEALTH, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	60889978838332 [Primary]

FDA Product Code

• EAM: Screen, intensifying, radiographic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-16

On-Brand Devices [MIN-R EV 150 Screen]

• 60889978838332: SGL 18X24CM MINR EV150 S WO FM FOEM
• 60889978300877: SGL 24X30CM MINR EV150 S WO FM FOEM