BECKMAN RETRACTOR 230-4901

GUDID 00192896096233

BECKMAN RETRACTOR HINGED SHARP PRONGS

SONTEC INSTRUMENTS, INC.

Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00192896096233
• NIH Device Record Key: 6ad91537-7bc8-4643-9328-bd6c2473c5f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BECKMAN RETRACTOR
• Version Model Number: 230-4901
• Catalog Number: 230-4901
• 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

Device Dimensions

• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896096233 [Primary]

FDA Product Code

• GAD: Retractor

Sterilization

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

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896096233]

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: 2019-05-16
• Device Publish Date: 2019-05-08

On-Brand Devices [BECKMAN RETRACTOR]

• 00192896026759: BECKMAN RETRACTOR HINGED SHARP TIPS
• 00192896096233: BECKMAN RETRACTOR HINGED SHARP PRONGS
• 00192896122567: Beckman Retractor Hinged 3 x 4 Sharp Prongs Enclosed Ratchet