DANIEL ENDOSCOPIC FOREHEAD SUCTION ELEVATOR

GUDID B0994783700

DANIEL ENDOSCOPIC FOREHEAD SUCTION ELEVATOR SLIGHT CURVED

SONTEC INSTRUMENTS, INC.

ENT elevator

• Primary Device ID: B0994783700
• NIH Device Record Key: d2c47131-6e5e-40fd-a88d-baf2dd85685f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DANIEL ENDOSCOPIC FOREHEAD SUCTION ELEVATOR
• Version Model Number: 478-370
• 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
• 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	00192896043480 [Primary]
HIBCC	B0994783700 [Previous]

FDA Product Code

• KAD: Elevator, Ent

Sterilization

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

[B0994783700]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0994783700]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0994783700]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-07-12
• Device Publish Date: 2018-09-06

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