Micasept Fenestrated Grasping Forceps 20920-15-004

GUDID 00192896118300

Micasept Fenestrated Grasping Forceps Rhombic Curved Left With Clamp Ratchet

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable

• Primary Device ID: 00192896118300
• NIH Device Record Key: 20e7cfcd-5c10-47eb-86a6-73d9f096c290
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micasept Fenestrated Grasping Forceps
• Version Model Number: 20920-15-004
• Catalog Number: 20920-15-004
• 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

• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 10 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896118300 [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

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

[00192896118300]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-06
• Device Publish Date: 2024-07-29

On-Brand Devices [Micasept Fenestrated Grasping Forceps]

• 00192896011106: MICASEPT FENESTRATED GRASPING FORCEPS PISTOL GRIP WITH RATCHET
• 00192896110601: Micasept Fenestrated Grasping Forceps Concave Y-Grip With French Ratchet
• 00192896110595: Micasept Fenestrated Grasping Forceps Y-Grip With Ratchet
• 00192896118218: Micasept Fenestrated Grasping Forceps Rhombic Curved Left With Clamp Ratchet
• 00192896118300: Micasept Fenestrated Grasping Forceps Rhombic Curved Left With Clamp Ratchet