Micasept Ciradur Scissors 20925-06

GUDID 00192896115262

Micasept Ciradur Scissors Blunt/Blunt Up Opening 30 Degrees Curved Down

SONTEC INSTRUMENTS, INC.

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• Primary Device ID: 00192896115262
• NIH Device Record Key: 43fc3644-fd04-4adf-a1d7-81aa25a79a17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micasept Ciradur Scissors
• Version Model Number: 20925-06
• Catalog Number: 20925-06
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter
• Lumen/Inner Diameter: 4.5 Millimeter
• Length: 300 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896115262 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K002877

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115262]

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: 2023-08-15
• Device Publish Date: 2023-08-07

On-Brand Devices [Micasept Ciradur Scissors]

• 00192896092242: MICASEPT CIRADUR SCISSORS WITH Y-GRIP STRAIGHT BLADE
• B09920928530: MICASEPT CIRADUR METZENBAUM SCISSORS MONOPOLAR CURVED LEFT SIDE OPENING
• 00192896115262: Micasept Ciradur Scissors Blunt/Blunt Up Opening 30 Degrees Curved Down