PIN PULLING PLIERS 1100-532

GUDID 00192896048010

PIN PULLING PLIERS DOUBLE ACTION TUNGSTEN CARBIDE SERRATED TIP

SONTEC INSTRUMENTS, INC.

Orthopaedic joint/limb rongeur

• Primary Device ID: 00192896048010
• NIH Device Record Key: 355c1a0b-cffb-4ce3-a16c-8d6d0cfe4f7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PIN PULLING PLIERS
• Version Model Number: 1100-532
• Catalog Number: 1100-532
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 7 Inch
• Length: 7 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896048010 [Primary]

FDA Product Code

• EJY: Pliers, operative
• HWB: Extractor

Sterilization

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

[00192896048010]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-12
• Device Publish Date: 2018-09-12

On-Brand Devices [PIN PULLING PLIERS]

• 00192896053922: PIN PULLING PLIERS TUNGSTEN CARBIDE TIP
• 00192896048027: PIN PULLING PLIERS DOUBLE ACTON TUNGSTEN CARBIDE SERRATED TIP
• 00192896048010: PIN PULLING PLIERS DOUBLE ACTION TUNGSTEN CARBIDE SERRATED TIP
• 00192896111615: Pin Pulling Pliers Double Action Tungsten Carbide Serrated