HIGH RESOLUTION OPTICS C-000.32.507

GUDID 00192896092655

HIGH RESOLUTION OPTICS BLACK

SONTEC INSTRUMENTS, INC.

Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe Loupe

• Primary Device ID: 00192896092655
• NIH Device Record Key: 7bce0630-e4ef-4840-85df-2d08be428ff4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HIGH RESOLUTION OPTICS
• Version Model Number: C-000.32.507
• Catalog Number: C-000.32.507
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0
• Length: 420 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896092655 [Primary]

FDA Product Code

• FSP: LOUPE, DIAGNOSTIC/SURGICAL

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-04
• Device Publish Date: 2019-01-03

On-Brand Devices [HIGH RESOLUTION OPTICS]

• 00192896092655: HIGH RESOLUTION OPTICS BLACK
• 00192896071308: HIGH RESOLUTION OPTICS