Imaging Extension, Short, OPERON D 750-D 8000045

GUDID 10841962110485

Imaging Extension, Short, OPERON D 750-D

Qfix

Universal operating table top

• Primary Device ID: 10841962110485
• NIH Device Record Key: d01d0462-efea-47e2-8011-3e19e87df8c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Imaging Extension, Short, OPERON D 750-D
• Version Model Number: 8000045
• Catalog Number: 8000045
• Company DUNS: 808875397
• Company Name: Qfix
• 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: false
• Serial Number: true
• 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(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com
• Phone: +1(610)268-0585
• Email: Compliance@qfix.com

Device Dimensions

• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Width: 21 Inch
• Length: 36 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841962110485 [Primary]

FDA Product Code

• KXJ: Table, radiologic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-12-11
• Device Publish Date: 2017-05-26

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