U.S. ARMY-NAVY RETRACTOR 1100-670

GUDID 00192896049406

U.S. ARMY-NAVY RETRACTOR

SONTEC INSTRUMENTS, INC.

Nerve/vessel retractor

• Primary Device ID: 00192896049406
• NIH Device Record Key: f7012a7b-6107-4d04-bcd0-01c581729ca2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: U.S. ARMY-NAVY RETRACTOR
• Version Model Number: 1100-670
• Catalog Number: 1100-670
• 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

• Length: 8.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896049406 [Primary]

FDA Product Code

• EIG: RETRACTOR, ALL TYPES
• GAD: Retractor

Sterilization

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

[00192896049406]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-05-22
• Device Publish Date: 2018-09-14

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