HAYES INTESTINAL CLAMP 10-0567

GUDID 00192896072091

HAYES INTESTINAL CLAMP ATRAUMATIC JAW

SONTEC INSTRUMENTS, INC.

Pylorus separator

• Primary Device ID: 00192896072091
• NIH Device Record Key: b1970427-d7de-4be8-882f-93f1e0acc134
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HAYES INTESTINAL CLAMP
• Version Model Number: 10-0567
• Catalog Number: 10-0567
• 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: 12.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896072091 [Primary]

FDA Product Code

• FFR: DEVICE, LOCKING, FOR INTESTINAL CLAMP

Sterilization

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

[00192896072091]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-05-15
• Device Publish Date: 2018-09-19

On-Brand Devices [HAYES INTESTINAL CLAMP]

• 00192896072091: HAYES INTESTINAL CLAMP ATRAUMATIC JAW
• 00192896011526: HAYES INTESTINAL CLAMP ANGLED TIP