RINSING CANNULA SC95-03296

GUDID 00192896054189

RINSING CANNULA WITHOUT STOPCOCK

SONTEC INSTRUMENTS, INC.

Surgical drill guide obturator

• Primary Device ID: 00192896054189
• NIH Device Record Key: 3a8e4f98-6fcb-43b4-856d-101818d6432c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RINSING CANNULA
• Version Model Number: SC95-03296
• Catalog Number: SC95-03296
• 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
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896054189 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896054189]

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: 2019-06-05
• Device Publish Date: 2019-05-28

On-Brand Devices [RINSING CANNULA]

• 00192896093232: RINSING CANNULA WITH STOPCOCK
• 00192896089587: RINSING CANNULA WITH STOP COCK
• 00192896054189: RINSING CANNULA WITHOUT STOPCOCK
• 00192896100794: RINSING CANNULA WITH STOPCOCK