Ring Curette 2900-215

GUDID 00192896120068

Ring Curette Sharp

SONTEC INSTRUMENTS, INC.

Bone curette, reusable

• Primary Device ID: 00192896120068
• NIH Device Record Key: 9df1f325-95f3-4414-a2d0-b135c9930f72
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ring Curette
• Version Model Number: 2900-215
• Catalog Number: 2900-215
• 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
• 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

• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Device Size Text, specify: 0
• Length: 270 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896120068 [Primary]

FDA Product Code

• HTF: CURETTE

Sterilization

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

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

[00192896120068]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-21
• Device Publish Date: 2024-10-11

On-Brand Devices [Ring Curette]

• 00192896093690: RING CURETTE ANGLED TIP ARTHROSCOPIC HANDLE
• 00192896120105: Ring Curette Sharp
• 00192896120099: Ring Curette Sharp
• 00192896120082: Ring Curette Sharp
• 00192896120075: Ring Curette Sharp
• 00192896120068: Ring Curette Sharp
• 00192896120051: Ring Curette Sharp
• 00192896120044: Ring Curette Sharp
• 00192896120037: Ring Curette Sharp
• 00192896120020: Ring Curette Blunt
• 00192896120013: Ring Curette Blunt
• 00192896120006: Ring Curette Blunt
• 00192896119994: Ring Curette Blunt
• 00192896119987: Ring Curette Blunt
• 00192896119970: Ring Curette Blunt
• 00192896119963: Ring Curette Blunt
• 00192896119956: Ring Curette Blunt