CURIX OPTHOS H 35ZQ7

GUDID 05414904024430

CURIX CAS EU+OPTHOS H 35X43

AGFA

X-ray film cassette, manual

• Primary Device ID: 05414904024430
• NIH Device Record Key: afc82a22-d560-4d88-977a-6e5ab6895d3d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CURIX OPTHOS H
• Version Model Number: CURIX OPTHOS H 35X43
• Catalog Number: 35ZQ7
• Company DUNS: 374444883
• Company Name: AGFA
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: +1(877)777-2432
• Email: salesinfo@agfa.com

Device Dimensions

• Width: 43 Centimeter
• Width: 43 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	05414904024430 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K023020

FDA Product Code

• IXA: Cassette, radiographic film

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-06-14
• Device Publish Date: 2016-09-01

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