SONTEC STIFLE THRUST LEVER 1100-6692

GUDID 00192896081932

SONTEC STIFLE THRUST LEVER

SONTEC INSTRUMENTS, INC.

Nerve/vessel retractor

• Primary Device ID: 00192896081932
• NIH Device Record Key: 974e74ef-e4b9-4fdf-8d4f-e5e43c68c3d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONTEC STIFLE THRUST LEVER
• Version Model Number: 1100-6692
• Catalog Number: 1100-6692
• 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: 11 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896081932 [Primary]

FDA Product Code

• EIG: RETRACTOR, ALL TYPES
• GAD: Retractor

Sterilization

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

[00192896081932]

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: 2018-09-21

On-Brand Devices [SONTEC STIFLE THRUST LEVER]

• 00192896081932: SONTEC STIFLE THRUST LEVER
• 00192896049383: SONTEC STIFLE THRUST LEVER