LaproGlide

GUDID 00860009758308

Laparoscopic L-Hook Electrode, 33cm Length, PTFE

Surgical Principals, Inc

Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use Open-surgery electrosurgical electrode, monopolar, single-use

• Primary Device ID: 00860009758308
• NIH Device Record Key: 8b1986d0-9c63-4e92-877b-8991dbff8a67
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LaproGlide
• Version Model Number: U0020
• Company DUNS: 782873892
• Company Name: Surgical Principals, Inc
• Device Count: 5
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00860009758308 [Unit of Use]
GS1	10860009758305 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-28
• Device Publish Date: 2024-05-20

On-Brand Devices [LaproGlide]

• 00860009758391: Laparoscopic L- Wire Electrode, 33cm Length, Foot Control, PTFE
• 00860009758384: Laparoscopic Round Spatula Electrode, 33cm Length, PTFE
• 00860009758377: Laparoscopic L- Wire Electrode, 45cm Length, PTFE
• 00860009758360: Laparoscopic L-Hook Electrode, 33cm Length, Foot Control, PTFE
• 00860009758353: Laparoscopic L-Wire Electrode, 33cm Length, PTFE
• 00860009758346: Laparoscopic L-Hook Electrode, 45cm Length, PTFE
• 00860009758339: Laparoscopic J-Hook Electrode, 45cm Length, PTFE
• 00860009758322: Laparoscopic Curved Blade Electrode, 33cm Length, PTFE
• 00860009758315: Laparoscopic J-Hook Electrode, 33cm Length, PTFE
• 00860009758308: Laparoscopic L-Hook Electrode, 33cm Length, PTFE