Micasept Organ Grasping Forceps 20919-03-014

GUDID 00192896111196

Micasept Organ Grasping Forceps Wide With Hegar Ratchet Fenestrated Straight

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable

• Primary Device ID: 00192896111196
• NIH Device Record Key: 19cb8acc-ee74-4e02-81f3-2ae5802ddbe1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micasept Organ Grasping Forceps
• Version Model Number: 20919-03-014
• Catalog Number: 20919-03-014
• 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

Device Dimensions

• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter
• Length: 300 Millimeter
• Outer Diameter: 6 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896111196 [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

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

Dry Heat Sterilization

[00192896111196]

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

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