COLLIN-DUVAL INTESTINAL CLAMP

GUDID 00192896100503

COLLIN-DUVAL INTESTINAL CLAMP SERRATED

SONTEC INSTRUMENTS, INC.

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

• Primary Device ID: 00192896100503
• NIH Device Record Key: c8c54b3c-b404-4084-8edb-53f107c215e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COLLIN-DUVAL INTESTINAL CLAMP
• Version Model Number: 2200-600
• 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: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 11 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896100503 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

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

[00192896100503]

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: 2020-01-14
• Device Publish Date: 2020-01-06

On-Brand Devices [COLLIN-DUVAL INTESTINAL CLAMP]

• 00192896100503: COLLIN-DUVAL INTESTINAL CLAMP SERRATED
• 00192896120136: Collin-Duval Intestinal Clamp Serrated