Micasept Fenestrated Grasping Forceps 20920-14-004

GUDID 00192896118218

Micasept Fenestrated Grasping Forceps Rhombic Curved Left With Clamp Ratchet

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable

• Primary Device ID: 00192896118218
• NIH Device Record Key: 9c712216-eb48-4155-8567-7bf1d91c1470
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micasept Fenestrated Grasping Forceps
• Version Model Number: 20920-14-004
• Catalog Number: 20920-14-004
• 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

Device Dimensions

• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 7 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 7 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 7 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 7 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 7 Millimeter
• Device Size Text, specify: 0
• Length: 300 Millimeter
• Width: 7 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896118218 [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

[00192896118218]

Dry Heat Sterilization

[00192896118218]

Dry Heat Sterilization

[00192896118218]

Dry Heat Sterilization

[00192896118218]

Dry Heat Sterilization

[00192896118218]

Dry Heat Sterilization

[00192896118218]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-11
• Device Publish Date: 2024-07-03

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