Aqua

GUDID 00858164002381

ELEKTA, INC.

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• Primary Device ID: 00858164002381
• NIH Device Record Key: f37c1eb2-acad-4ebe-9f83-ce35720fecb2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aqua
• Version Model Number: 3.0.2
• Company DUNS: 079089435
• Company Name: ELEKTA, INC.
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00858164002381 [Primary]

FDA Product Code

• LHO: Instrument, Quality-Assurance, Radiologic

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: 2023-06-30
• Device Publish Date: 2023-06-22

Devices Manufactured by ELEKTA, INC.

• 00858164002381 - Aqua: 2023-06-30
• 00858164002381 - Aqua: 2023-06-30
• 00858164002367 - MOSAIQ: 2021-12-10
• 00858164002336 - MOSAIQ: 2019-11-08
• 00858164002275 - Monaco: 2019-10-25
• 00858164002237 - MOSAIQ: 2019-08-12
• 00858164002251 - MOSAIQ: 2019-08-12
• 00858164002039 - Atlas-Based Autosegmentation: 2019-08-05
• 00858164002114 - XiO: 2019-08-05