LiNA SeaStar™ 4000-S-Q

GUDID 05708265002269

single use retractor ring; Squared model

Lina Medical ApS

Surgical retraction system mounting frame, single-use, sterile

• Primary Device ID: 05708265002269
• NIH Device Record Key: a53a0b4c-7fc4-40d5-8717-c6676582b019
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiNA SeaStar™
• Version Model Number: 4000-S-Q
• Catalog Number: 4000-S-Q
• Company DUNS: 305088619
• Company Name: Lina Medical ApS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Customer Support Contacts

• Phone: +48612222121
• Email: info.poland@lina-medical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05708265002269 [Primary]
GS1	05708265002276 [Package]; Package: box [5 Units]; In Commercial Distribution

FDA Product Code

• GAD: Retractor

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-15

On-Brand Devices [LiNA SeaStar™]

• 05708265002269: single use retractor ring; Squared model
• 05708265000883: single use retractor ring VV model (V-shape/V-shape)
• 05708265000876: single use retractor ring; VS model (V-shape/Small)
• 05708265000869: single use retractor ring; VL model (V-shape/Large)
• 05708265000852: single use retractor ring; SS model (Small/Small)
• 05708265000845: single use retractor ring; SL model (Small/Large)