BIPOLAR COAPTATION FORCEPS

GUDID B09927009300

BIPOLAR COAPTATION FORCEPS

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

• Primary Device ID: B09927009300
• NIH Device Record Key: 88c44de4-6099-4198-bd64-4122d799dae4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BIPOLAR COAPTATION FORCEPS
• Version Model Number: 2700-930
• 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
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 4.25 Inch
• Length: 4.25 Inch
• Length: 4.25 Inch
• Length: 4.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896100459 [Primary]
HIBCC	B09927009300 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101080

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[B09927009300]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927009300]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-14
• Device Publish Date: 2020-01-06

On-Brand Devices [BIPOLAR COAPTATION FORCEPS ]

• 00192896010802: BIPOLAR COAPTATION FORCEPS INSULATED
• B09927009300: BIPOLAR COAPTATION FORCEPS