Sontec Dubost Retractor Blade 2500-4992

GUDID 00192896116450

Sontec Dubost Retractor Blade Medium

SONTEC INSTRUMENTS, INC.

Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00192896116450
• NIH Device Record Key: ae455e8f-8c75-4298-a892-d69d3f0f402c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sontec Dubost Retractor Blade
• Version Model Number: 2500-4992
• Catalog Number: 2500-4992
• 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

Device Dimensions

• Width: 40 Millimeter
• Length: 100 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896116450 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00192896116450]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-19
• Device Publish Date: 2024-02-09

On-Brand Devices [Sontec Dubost Retractor Blade]

• 00192896116467: Sontec Dubost Retractor Blade Large
• 00192896116450: Sontec Dubost Retractor Blade Medium
• 00192896116443: Sontec Dubost Retractor Blade Small