GUBISCH SUCTION ELEVATOR 478-380

GUDID 00192896043510

GUBISCH SUCTION ELEVATOR STRAIGHT TIP

SONTEC INSTRUMENTS, INC.

ENT elevator

• Primary Device ID: 00192896043510
• NIH Device Record Key: 20e9dbaa-a506-4b64-93b7-6cd678bab75a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GUBISCH SUCTION ELEVATOR
• Version Model Number: 478-380
• Catalog Number: 478-380
• 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: 6 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896043510 [Primary]

FDA Product Code

• KAD: ELEVATOR, ENT

Sterilization

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

[00192896043510]

Moist Heat or Steam Sterilization;Dry Heat 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: 2018-09-14

On-Brand Devices [GUBISCH SUCTION ELEVATOR]

• 00192896043527: GUBISCH SUCTION ELEVATOR BAYONET STRAIGHT TIP
• 00192896043510: GUBISCH SUCTION ELEVATOR STRAIGHT TIP