CUSHING RETRACTOR 2500-350

GUDID 00192896086821

CUSHING RETRACTOR

SONTEC INSTRUMENTS, INC.

Rib spreader, reusable

• Primary Device ID: 00192896086821
• NIH Device Record Key: ef465074-ce61-428e-b197-be103284a489
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CUSHING RETRACTOR
• Version Model Number: 2500-350
• Catalog Number: 2500-350
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896086821 [Primary]

FDA Product Code

• FGN: RETRACTOR, NON-SELF-RETAINING

Sterilization

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

[00192896086821]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-06
• Device Publish Date: 2018-09-24

On-Brand Devices [CUSHING RETRACTOR]

• 00192896086852: CUSHING RETRACTOR WIDE HANDLE
• 00192896086845: CUSHING RETRACTOR
• 00192896086838: CUSHING RETRACTOR
• 00192896086821: CUSHING RETRACTOR