Egress Cannula

GUDID 00192896110830

Egress Cannula With Conical Obturator 7.1 Millimeter Inner Diameter

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 00192896110830
• NIH Device Record Key: a4bf20c3-7ad7-4dfb-aaef-6596f33ba76a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Egress Cannula
• Version Model Number: 2100-575A
• 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: 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

Device Dimensions

• Length: 12 Inch
• Length: 12 Inch
• Length: 12 Inch
• Length: 12 Inch
• Length: 12 Inch
• Length: 12 Inch
• Length: 12 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896110830 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092544

FDA Product Code

• DXC: CLAMP, VASCULAR

Sterilization

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

[00192896110830]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110830]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110830]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110830]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110830]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110830]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110830]

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: 2021-08-09
• Device Publish Date: 2021-07-30

On-Brand Devices [Egress Cannula]

• 00192896087842: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896087835: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896087828: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896087811: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896087804: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896070608: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896070592: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896070585: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896100428: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896104730: Egress Cannula With Conical Obturator 8.1 Millimeter Inner Diameter
• 00192896110830: Egress Cannula With Conical Obturator 7.1 Millimeter Inner Diameter
• 00192896110984: Egress Cannula With Conical Obturator
• 00192896110977: Egress Cannula With Conical Obturator
• 00192896115552: Egress Cannula With Conical Obturator