SONTEC KNIFE HANDLE 1100-8681

GUDID 00192896082236

SONTEC KNIFE HANDLE #3XXL

SONTEC INSTRUMENTS, INC.

Scalpel handle, reusable

• Primary Device ID: 00192896082236
• NIH Device Record Key: e631137b-a5bb-403d-9978-61335b0eda5b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONTEC KNIFE HANDLE
• Version Model Number: 1100-8681
• Catalog Number: 1100-8681
• 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: 16 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896082236 [Primary]

FDA Product Code

• EMF: KNIFE, SURGICAL
• GDZ: Handle, Scalpel

Sterilization

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

[00192896082236]

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: 2019-03-08
• Device Publish Date: 2018-09-21

On-Brand Devices [SONTEC KNIFE HANDLE ]

• 00192896082236: SONTEC KNIFE HANDLE #3XXL
• 00192896049949: SONTEC KNIFE HANDLE #4L
• 00192896049925: SONTEC KNIFE HANDLE #3L