HOKE RETRACTOR 207-201

GUDID 00192896092785

HOKE RETRACTOR

SONTEC INSTRUMENTS, INC.

Hand-held surgical retractor, reusable

• Primary Device ID: 00192896092785
• NIH Device Record Key: dd1f6c85-f0c4-4de3-8d83-a71df22ca680
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HOKE RETRACTOR
• Version Model Number: 207-201
• Catalog Number: 207-201
• 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

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896092785 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00192896092785]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-04
• Device Publish Date: 2019-01-03

On-Brand Devices [HOKE RETRACTOR]

• 00192896092785: HOKE RETRACTOR
• 00192896092778: HOKE RETRACTOR