MCPHERSON BIPOLAR FORCEPS

GUDID B0991627100

MCPHERSON BIPOLAR FORCEPS ANGLED TYPE PLATFORM

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

• Primary Device ID: B0991627100
• NIH Device Record Key: 10edb7b4-253b-4c45-989d-d597faba3dee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MCPHERSON BIPOLAR FORCEPS
• Version Model Number: 16-2710
• 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

Device Dimensions

• Length: 94 Millimeter
• Length: 94 Millimeter
• Length: 94 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896000254 [Primary]
HIBCC	B0991627100 [Previous]

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

[B0991627100]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991627100]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991627100]

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: 2018-09-20
• Device Publish Date: 2018-08-20

On-Brand Devices [MCPHERSON BIPOLAR FORCEPS ]

• B0991627100: MCPHERSON BIPOLAR FORCEPS ANGLED TYPE PLATFORM
• B0991627000: MCPHERSON BIPOLAR FORCEPS SMOOTH TYING PLATFORM STRAIGHT TIP