RINSING CANNULA SC95-03296

GUDID 00192896054189

RINSING CANNULA WITHOUT STOPCOCK

SONTEC INSTRUMENTS, INC.

Surgical drill guide obturator Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable Arthroscopic access cannula, reusable

• 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