MCGIVNEY ALLIS HEMORRHOID FORCEPS

GUDID B099508553R0

MCGIVNEY ALLIS HEMORRHOID FORCEPS ANGLED SHANK/ JAW

SONTEC INSTRUMENTS, INC.

Open-surgery biopsy forceps, reusable

• Primary Device ID: B099508553R0
• NIH Device Record Key: 943f4833-08d0-4d42-83b3-79883770bcce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MCGIVNEY ALLIS HEMORRHOID FORCEPS
• Version Model Number: 508-553R
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896044739 [Primary]
HIBCC	B099508553R0 [Previous]

FDA Product Code

• FHN: Ligator, Hemorrhoidal
• GEN: Forceps, General & Plastic Surgery

Sterilization

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

[B099508553R0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B099508553R0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B099508553R0]

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: 2018-09-06

Devices Manufactured by SONTEC INSTRUMENTS, INC.

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