CARINA 0007536-0005

GUDID 04260590370600

L A P GMBH LASER APPLIKATIONEN

Laser patient positioning system

• Primary Device ID: 04260590370600
• NIH Device Record Key: 7032bdeb-2f12-4ef5-897e-f67257229fe2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CARINA
• Version Model Number: CARINAnav
• Catalog Number: 0007536-0005
• Company DUNS: 313586582
• Company Name: L A P GMBH LASER APPLIKATIONEN
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260590370600 [Primary]

FDA Product Code

• IWE: Monitor, Patient Position, Light-Beam

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-01
• Device Publish Date: 2019-01-01

On-Brand Devices [CARINA]

• 04260590370631: CARINAnav Desktop PC
• 04260590370624: CARINAnav (B)
• 04260590370617: CARINAnav (B)
• 04260590370600: CARINAnav
• 04260590370594: CARINAnav
• 04260590370587: CARINAsim DORADO
• 04260590370570: CARINAiso
• 04260590370730: CARINAnav Desktop PC
• 04260590370778: CARINAnav (E)
• 04260590370761: CARINAnav (E)