FORD DIXON LIGATOR

GUDID B0995085600

FORD DIXON LIGATOR WITH LOADING CONE & 100 O-RINGS

SONTEC INSTRUMENTS, INC.

Haemorrhoid ligator

• Primary Device ID: B0995085600
• NIH Device Record Key: 3486473b-bccc-4ec3-a908-1ddea0f7518f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORD DIXON LIGATOR
• Version Model Number: 508-560
• 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	00192896044760 [Primary]
HIBCC	B0995085600 [Previous]

FDA Product Code

• FHN: Ligator, Hemorrhoidal

Sterilization

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

[B0995085600]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0995085600]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0995085600]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-08
• Device Publish Date: 2018-09-06

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