TITANIUM FLEXIBLE TROCAR SET 20910-15

GUDID 00192896007833

TITANIUM FLEXIBLE TROCAR SET

SONTEC INSTRUMENTS, INC.

Laparoscopic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 00192896007833
• NIH Device Record Key: 74d42df0-dfdb-4c38-bba1-9aea11858e42
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TITANIUM FLEXIBLE TROCAR SET
• Version Model Number: 20910-15
• Catalog Number: 20910-15
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Device Dimensions

• Outer Diameter: 10.5 Millimeter
• Outer Diameter: 10.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896007833 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K002877

FDA Product Code

• HET: Laparoscope, Gynecologic (And Accessories)

Sterilization

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

[00192896007833]

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: 2018-09-17
• Device Publish Date: 2018-08-15

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