KILLIAN NASAL SPECULUM 465-325

GUDID 00192896097872

KILLIAN NASAL SPECULUM WITH FIBER OPTIC LIGHT GUIDE

SONTEC INSTRUMENTS, INC.

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• Primary Device ID: 00192896097872
• NIH Device Record Key: 859cb510-d08a-42b3-8813-09d069d595fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KILLIAN NASAL SPECULUM
• Version Model Number: 465-325
• Catalog Number: 465-325
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0
• Length: 5.5 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896097872 [Primary]

FDA Product Code

• EPY: Speculum, Ent

Sterilization

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

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896097872]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-02
• Device Publish Date: 2019-06-24

On-Brand Devices [KILLIAN NASAL SPECULUM]

• 00192896079618: KILLIAN NASAL SPECULUM WITH FIBER LIGHT GUIDE FIXATION SCREW
• 00192896079601: KILLIAN NASAL SPECULUM WITH FIBER LIGHT GUIDE FIXATION SCREW
• 00192896095670: KILLIAN NASAL SPECULUM WITH FIBER OPTIC LIGHT GUIDE FIXED SCREW
• 00192896097872: KILLIAN NASAL SPECULUM WITH FIBER OPTIC LIGHT GUIDE