Maryland Grasping Forceps 2901-262L

GUDID 00192896115040

Maryland Grasping Forceps Double Action Jaw Insert For 10 Millimeter Diameter Tube Shaft

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable

• Primary Device ID: 00192896115040
• NIH Device Record Key: 050bb67c-a47a-4e20-b691-d88a2bfde306
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Maryland Grasping Forceps
• Version Model Number: 2901-262L
• Catalog Number: 2901-262L
• 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

• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896115040 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102921

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896115040]

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: 2023-07-03
• Device Publish Date: 2023-06-23

On-Brand Devices [Maryland Grasping Forceps]

• B0992901202S0: MARYLAND GRASPING FORCEPS DOUBLE-ACTION JAWS FOR TUBE SHAFT
• B0992901202L0: MARYLAND GRASPING FORCEPS DOUBLE-ACTION JAWS FOR TUBE SHAFT
• 00192896115040: Maryland Grasping Forceps Double Action Jaw Insert For 10 Millimeter Diameter Tube Shaft