Micaspet Babcock Clamp/Node Grasper

GUDID 00192896108196

Micasept Babcock Clamp/Node Grasper With Round Ratchet Atraumatic 30 Degrees Curved Down 4.5 Millimeters

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 00192896108196
• NIH Device Record Key: e5020f7e-865c-482f-b01c-3d20d3a9dd1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micaspet Babcock Clamp/Node Grasper
• Version Model Number: 20919-12
• 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

Device Dimensions

• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter
• Length: 300 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896108196 [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

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896108196]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-13
• Device Publish Date: 2021-05-05

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