SPINAL FUSION CURETTE 320-860-9-0

GUDID 00192896077768

SPINAL FUSION CURETTE STRAIGHT TIP SIZE 0

SONTEC INSTRUMENTS, INC.

Bone curette, reusable

• Primary Device ID: 00192896077768
• NIH Device Record Key: 65882244-be82-4ce4-baf3-f59b406a6c70
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPINAL FUSION CURETTE
• Version Model Number: 320-860-9-0
• Catalog Number: 320-860-9-0
• 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: 9 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896077768 [Primary]

FDA Product Code

• HTF: CURETTE

Sterilization

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

[00192896077768]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-05-07
• Device Publish Date: 2018-09-20

On-Brand Devices [SPINAL FUSION CURETTE]

• 00192896077768: SPINAL FUSION CURETTE STRAIGHT TIP SIZE 0
• 00192896101838: Spinal Fusion Curette Straight Tip
• 00192896101821: Spinal Fusion Curette Straight Tip
• 00192896101814: Spinal Fusion Curette Straight Tip
• 00192896101807: Spinal Fusion Curette Straight Tip