Kelly Retractor 207-356

GUDID 00192896120785

Kelly Retractor Lamb Handle

SONTEC INSTRUMENTS, INC.

Hand-held surgical retractor, reusable

• Primary Device ID: 00192896120785
• NIH Device Record Key: b7cba37a-94a6-4481-9713-1aae197c4abf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kelly Retractor
• Version Model Number: 207-356
• Catalog Number: 207-356
• 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

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896120785 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

[00192896120785]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-12
• Device Publish Date: 2024-11-04

On-Brand Devices [Kelly Retractor]

• 00192896025875: KELLY RETRACTOR HOLLOW GRIP HANDLE
• 00192896025868: KELLY RETRACTOR HOLLOW GRIP HANDLE
• 00192896109445: Kelly Retractor 160 X 38 Millimeters
• 00192896120785: Kelly Retractor Lamb Handle