Kitzmiller Forceps

GUDID 00192896110137

Kitzmiller Forceps Cooley Jaws Angled Left Titanium

SONTEC INSTRUMENTS, INC.

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

• Primary Device ID: 00192896110137
• NIH Device Record Key: 09d81877-e6c4-407b-9777-7700405e4600
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kitzmiller Forceps
• Version Model Number: 2600-100L
• 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: 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

Device Dimensions

• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch
• Length: 5.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896110137 [Primary]

FDA Product Code

• DWS: INSTRUMENTS, SURGICAL, CARDIOVASCULAR

Sterilization

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

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896110137]

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: 2021-06-09
• Device Publish Date: 2021-06-01

On-Brand Devices [Kitzmiller Forceps]

• 00192896098121: KITZMILLER FORCEPS RIGHT HANDED TITANIUM
• 00192896098114: KITZMILLER FORCEPS LEFT HANDED TITANIUM
• 00192896110144: Kitzmiller Forceps Cooley Jaws Angled Right Titanium
• 00192896110137: Kitzmiller Forceps Cooley Jaws Angled Left Titanium