MIS Inner Ear Suction Sickle Knife 412-939

GUDID 00192896121812

MIS Inner Ear Suction Sickle Knife 35 Degree Curved With Suction Hole 2.0 Millimeter

SONTEC INSTRUMENTS, INC.

Tympanotomy knife, reusable

• Primary Device ID: 00192896121812
• NIH Device Record Key: 4a44114a-30e3-49bc-9920-a83ebbe892c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MIS Inner Ear Suction Sickle Knife
• Version Model Number: 412-939
• Catalog Number: 412-939
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter
• Length: 130 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896121812 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

[00192896121812]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-25
• Device Publish Date: 2025-07-17

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