LiNA PowerBlade™

GUDID 05708265001088

LiNA PowerBlade, Bipolar cutting & coagulation forceps, curved jaws, Ø 5,4mm, 185 mm working length, 3m cable, EURO connector

Lina Medical ApS

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: 05708265001088
• NIH Device Record Key: 15708cca-d96e-486b-926c-0a8deabf02bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiNA PowerBlade™
• Version Model Number: 5005-E-C-160
• Company DUNS: 305088619
• Company Name: Lina Medical ApS
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05708265001071 [Primary]
GS1	05708265001088 [Package]; Contains: 05708265001071; Package: box [5 Units]; In Commercial Distribution

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: 2023-06-15
• Device Publish Date: 2023-06-07

On-Brand Devices [LiNA PowerBlade™ ]

• 05708265001040: Bipolar Cutting & Coagulation forceps, 5mm, 3m cable, 4mm pins, curved jaws and knife, length 16
• 05708265001026: Bipolar Cutting & Coagulation forceps, 5mm, 3m cable, 4mm pins, straight, length 160mm
• 05708265000685: Bipolar Cutting & Coagulation forceps, 10mm, 3m cable, 4mm pins, straight, length 160mm, for Ope
• 05708265000678: Bipolar Cutting & Coagulation forceps, 10mm, 3m cable, 4mm pins, straight, length 320mm
• 05708265000654: Bipolar Cutting & Coagulation forceps, 5mm, 3m cable, 4mm pins, curved jaws and knife, length 33
• 05708265000647: Bipolar Cutting & Coagulation forceps, 5mm, 3m cable, 4mm pins, straight, length 420mm
• 05708265000630: Bipolar Cutting & Coagulation forceps, 5mm, 3m cable, 4mm pins, straight, length 330mm
• 05708265005949: LiNA PowerBlade, Bipolar cutting & coagulation forceps, straight jaws, Ø 10mm, 185 mm working l
• 05708265005932: LiNA PowerBlade, Bipolar cutting & coagulation forceps, straight jaws, Ø 10mm, 330 mm working l
• 05708265004454: LiNA PowerBlade, Bipolar cutting & coagulation forceps, curved jaws, Ø 5,4mm, 330 mm working le
• 05708265004430: LiNA PowerBlade, Bipolar cutting & coagulation forceps, straight jaws, Ø 10mm, 330 mm working l
• 05708265001088: LiNA PowerBlade, Bipolar cutting & coagulation forceps, curved jaws, Ø 5,4mm, 185 mm working le