COOLEY DERRA CLAMP

GUDID 00192896101708

COOLEY DERRA CLAMP CURVED TIP LARGE SIZE

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 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: 00192896101708
• NIH Device Record Key: a190e80f-6454-4fb4-8b8d-fea6b905b46a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COOLEY DERRA CLAMP
• Version Model Number: 2100-349Q
• 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
• 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: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch
• Length: 6.75 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896101708 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092544

FDA Product Code

• DXC: CLAMP, VASCULAR

Sterilization

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

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896101708]

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: 2020-05-26
• Device Publish Date: 2020-05-18

On-Brand Devices [COOLEY DERRA CLAMP]

• B09921003550: COOLEY DERRA CLAMP SMALL JAW
• B09921003450: COOLEY DERRA CLAMP CURVED SMALL
• B09921003490: COOLEY DERRA CLAMP CURVED LARGE
• B09921003470: COOLEY DERRA CLAMP CURVED MEDIUM
• B09921003600: COOLEY DERRA CLAMP ATRAUMATIC LARGE JAW
• 00192896101708: COOLEY DERRA CLAMP CURVED TIP LARGE SIZE