BE-ST Bipolar Forceps

GUDID 00853508002065

Bayonet Bipolar Forceps, Straight Tip

LACEY MANUFACTURING COMPANY, LLC

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

• Primary Device ID: 00853508002065
• NIH Device Record Key: a7a44c9a-1d84-47bb-ba3a-7f9549e8cc7c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BE-ST Bipolar Forceps
• Version Model Number: 1590-03
• Company DUNS: 958212029
• Company Name: LACEY MANUFACTURING COMPANY, LLC
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch
• Length: 11.6 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853508002065 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131058

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-04-23
• Device Publish Date: 2016-09-19

On-Brand Devices [BE-ST Bipolar Forceps]

• 00853508002096: Bayonet Bipolar Forceps Straight Tip
• 00853508002065: Bayonet Bipolar Forceps, Straight Tip
• 00853508002058: Bayonet Bipolar Forceps, Angled Tip
• 00853508002034: Electrosurgical Bipolar Device