USA RING CURETTE 320-922B

GUDID 00192896077911

USA RING CURETTE STRAIGHT RING SIZE 3 PHENOLIC HANDLE

SONTEC INSTRUMENTS, INC.

Bone curette, reusable

• Primary Device ID: 00192896077911
• NIH Device Record Key: 26ff98ce-c6a5-49b1-8f2a-22e827f4f184
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: USA RING CURETTE
• Version Model Number: 320-922B
• Catalog Number: 320-922B
• 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: 10 Inch
• Length: 10 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896077911 [Primary]

FDA Product Code

• HTF: CURETTE

Sterilization

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

[00192896077911]

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 [USA RING CURETTE]

• 00192896077928: USA RING CURETTE STRAIGHT RING SIZE 4 PHENOLIC HANDLE
• 00192896077911: USA RING CURETTE STRAIGHT RING SIZE 3 PHENOLIC HANDLE
• 00192896101739: USA RING CURETTE STRAIGHT TIP PHENOLIC HANDLE