Omni

GUDID 00195278592309

OMNI GANTRY 24-30 INCL. ELECTRONICS ASSY

G E MEDICAL SYSTEMS ISRAEL LTD.

Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system Full-body CT system

• Primary Device ID: 00195278592309
• NIH Device Record Key: 50a3af3c-54ef-4706-bbc4-1b6a1d9e5b81
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Omni
• Version Model Number: Legend
• Company DUNS: 532102365
• Company Name: G E MEDICAL SYSTEMS ISRAEL LTD.
• 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: false
• Lot Batch: true
• 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

Customer Support Contacts

• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00195278592309 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K221932

FDA Product Code

• KPS: System, tomography, computed, emission

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: 2022-09-20
• Device Publish Date: 2022-09-12

Devices Manufactured by G E MEDICAL SYSTEMS ISRAEL LTD.

• 00195278794772 - D630 to D670 DR Upgrade: 2024-03-26 D630 to D670 DR NM GANTRY UPGRADE KIT
• 00195278788252 - NM: 2023-11-23 830 NM GANTRY FINAL WITH NEW ROTOR - MDR CE
• 00195278788269 - NMCT: 2023-11-22 870 DR NM GANTRY FINAL WITH NEW ROTOR - MDR CE
• 00195278488619 - MyoSPECT: 2023-09-22 MyoSPECT MDR GANTRY
• 00195278488626 - MyoSPECT ES: 2023-09-22 MyoSPECT ES MDR GANTRY
• 00195278722546 - MyoSEPCT ES to MyoSPECT Upgrade: 2023-09-22 MyoSPECT ES to MyoSPECT Upgrade kit
• 00195278592309 - Omni: 2022-09-20OMNI GANTRY 24-30 INCL. ELECTRONICS ASSY
• 00195278592309 - Omni: 2022-09-20 OMNI GANTRY 24-30 INCL. ELECTRONICS ASSY
• 00195278421579 - MyoSPECT ES: 2021-10-19 MyoSPECT ES GANTRY