USA RING CURETTE

GUDID 00192896101739

USA RING CURETTE STRAIGHT TIP PHENOLIC HANDLE

SONTEC INSTRUMENTS, INC.

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable

• Primary Device ID: 00192896101739
• NIH Device Record Key: d6d61fd3-6e12-42a8-92b4-4d8dfd899a13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: USA RING CURETTE
• Version Model Number: 320-922A
• 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
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch
• Device Size Text, specify: 0
• Length: 10 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896101739 [Primary]

FDA Product Code

• HTF: CURETTE

Sterilization

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

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896101739]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-26
• Device Publish Date: 2020-05-18

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